Erratum: Correction to: Recessive VARS2 mutation underlies a novel syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadism (Human genomics (2017) 11 1 (28))

Abdulaziz Alsemari; Banan Al-Younes; Ewa Goljan; Dyala Jaroudi; Faisal BinHumaid; Brian F. Meyer; Stefan T. Arold; Dorota Monies

doi:10.1186/s40246-017-0130-6

Erratum: Correction to: Recessive VARS2 mutation underlies a novel syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadism (Human genomics (2017) 11 1 (28))

Abdulaziz Alsemari, Banan Al-Younes, Ewa Goljan, Dyala Jaroudi, Faisal BinHumaid, Brian F. Meyer, Stefan T. Arold, Dorota Monies

Research output: Contribution to journal › Comment/debate › peer-review

1 Scopus citations

Abstract

CORRECTION: After publication of the article [1], it has been brought to our attention that there is a nomenclature issue with this article. At the time of acceptance, the VARS2 mutation was considered equivalent to the VARS2 mutation. However, this has changed so that VARS now only refers to shorter mitochondrial sequence of valyl-tRNA synthesase containing 1093 amino acids. "Therefore, in the context of this article, every usage of "VARS2" should be replaced with "VARS" when referring to the causative variant".

Original language	English (US)
Pages (from-to)	33
Number of pages	1
Journal	Human Genomics
Volume	11
Issue number	1
DOIs	https://doi.org/10.1186/s40246-017-0130-6
State	Published - Dec 8 2017

ASJC Scopus subject areas

Molecular Medicine
Molecular Biology
Genetics
Drug Discovery

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Alsemari, A., Al-Younes, B., Goljan, E., Jaroudi, D., BinHumaid, F., Meyer, B. F., Arold, S. T., & Monies, D. (2017). Erratum: Correction to: Recessive VARS2 mutation underlies a novel syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadism (Human genomics (2017) 11 1 (28)). Human Genomics, 11(1), 33. https://doi.org/10.1186/s40246-017-0130-6

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title = "Erratum: Correction to: Recessive VARS2 mutation underlies a novel syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadism (Human genomics (2017) 11 1 (28))",

abstract = "CORRECTION: After publication of the article [1], it has been brought to our attention that there is a nomenclature issue with this article. At the time of acceptance, the VARS2 mutation was considered equivalent to the VARS2 mutation. However, this has changed so that VARS now only refers to shorter mitochondrial sequence of valyl-tRNA synthesase containing 1093 amino acids. {"}Therefore, in the context of this article, every usage of {"}VARS2{"} should be replaced with {"}VARS{"} when referring to the causative variant{"}.",

author = "Abdulaziz Alsemari and Banan Al-Younes and Ewa Goljan and Dyala Jaroudi and Faisal BinHumaid and Meyer, {Brian F.} and Arold, {Stefan T.} and Dorota Monies",

year = "2017",

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day = "8",

doi = "10.1186/s40246-017-0130-6",

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Alsemari, A, Al-Younes, B, Goljan, E, Jaroudi, D, BinHumaid, F, Meyer, BF, Arold, ST & Monies, D 2017, 'Erratum: Correction to: Recessive VARS2 mutation underlies a novel syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadism (Human genomics (2017) 11 1 (28))', Human Genomics, vol. 11, no. 1, pp. 33. https://doi.org/10.1186/s40246-017-0130-6

Erratum: Correction to: Recessive VARS2 mutation underlies a novel syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadism (Human genomics (2017) 11 1 (28)). / Alsemari, Abdulaziz; Al-Younes, Banan; Goljan, Ewa et al.
In: Human Genomics, Vol. 11, No. 1, 08.12.2017, p. 33.

Research output: Contribution to journal › Comment/debate › peer-review

TY - JOUR

T1 - Erratum

T2 - Correction to: Recessive VARS2 mutation underlies a novel syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadism (Human genomics (2017) 11 1 (28))

AU - Alsemari, Abdulaziz

AU - Al-Younes, Banan

AU - Goljan, Ewa

AU - Jaroudi, Dyala

AU - BinHumaid, Faisal

AU - Meyer, Brian F.

AU - Arold, Stefan T.

AU - Monies, Dorota

PY - 2017/12/8

Y1 - 2017/12/8

N2 - CORRECTION: After publication of the article [1], it has been brought to our attention that there is a nomenclature issue with this article. At the time of acceptance, the VARS2 mutation was considered equivalent to the VARS2 mutation. However, this has changed so that VARS now only refers to shorter mitochondrial sequence of valyl-tRNA synthesase containing 1093 amino acids. "Therefore, in the context of this article, every usage of "VARS2" should be replaced with "VARS" when referring to the causative variant".

AB - CORRECTION: After publication of the article [1], it has been brought to our attention that there is a nomenclature issue with this article. At the time of acceptance, the VARS2 mutation was considered equivalent to the VARS2 mutation. However, this has changed so that VARS now only refers to shorter mitochondrial sequence of valyl-tRNA synthesase containing 1093 amino acids. "Therefore, in the context of this article, every usage of "VARS2" should be replaced with "VARS" when referring to the causative variant".

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U2 - 10.1186/s40246-017-0130-6

DO - 10.1186/s40246-017-0130-6

M3 - Comment/debate

C2 - 29221463

AN - SCOPUS:85077170105

SN - 1473-9542

VL - 11

SP - 33

JO - Human Genomics

JF - Human Genomics

IS - 1

ER -

Erratum: Correction to: Recessive VARS2 mutation underlies a novel syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadism (Human genomics (2017) 11 1 (28))

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