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pro vyhledávání: '"Anastasiya L. Kungurtseva"'
Publikováno v:
Вопросы современной педиатрии, Vol 23, Iss 3, Pp 124-130 (2024)
Cockayne syndrome is a rare genetic disease from the group of premature aging syndromes associated with impaired DNA repair. The syndrome is autosomal recessive, and it is caused by pathogenic variants in ERCC8, ERCC6, XPB (ERCC3), XPD (ERCC2), and X
Externí odkaz:
https://doaj.org/article/9290706314b74667b1677c9d5dbe0b2c