Ошибки: Клинические и молекулярно-генетические характеристики пациентов с нарушением формирования пола 46,XY, обусловленным мутациями в гене NR5A1. [Проблемы эндокринологии 2020;66(3):62-69. doi: 10.14341/probl12445]

n the article some corrections were needed. Abstract: “Heterozygous SF1 variants were found in 36 out of 310 (11.6%) of cases, among them 15 were not previously described”. has been corrected to read “Heterozygous SF1 variants were found in 36 out of 310 (11.6%) of cases, among them 22 were not prev...

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Detalles Bibliográficos
Autores principales: Калинченко, Н. Ю., Колодкина, А. А., Райгородская, Н. Ю., Тюльпаков, А. Н.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrinology Research Centre 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9112850/
https://www.ncbi.nlm.nih.gov/pubmed/35018768
http://dx.doi.org/10.14341/probl12848

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9112850/
https://www.ncbi.nlm.nih.gov/pubmed/35018768
http://dx.doi.org/10.14341/probl12848

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