21-Hydroxylase deficiency associated with an atypical CYP21A2 E6 cluster containing p.I236K
Сохранить в:
Главные авторы: | Daisuke Watanabe (Автор), Hideaki Yagasaki (Автор), Satoru Kojika (Автор), Takeshi Inukai (Автор) |
---|---|
Формат: | |
Опубликовано: |
Elsevier,
2020-08-01T00:00:00Z.
|
Предметы: | |
Online-ссылка: | Connect to this object online. |
Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|
Схожие документы
-
Implications of CYP21A2 gene duplications in carrier screening and prenatal diagnosis of congenital adrenal hyperplasia due to 21 Hydroxylase deficiency
по: Sudhisha Dubey, и др.
Опубликовано: (2022) -
Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene
по: Ji-Hee Yoon, и др.
Опубликовано: (2024) -
Novel deletion alleles carrying <it>CYP21A1P</it>/<it>A2 </it>chimeric genes in Brazilian patients with 21-hydroxylase deficiency
по: Guerra-Júnior Gil, и др.
Опубликовано: (2010) -
Phenotype and genotype characteristics of Indonesian 21-hydroxylase deficient patients
по: Atiek Widya Oswari, и др.
Опубликовано: (2007) -
Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency
по: Helmuth G. Dörr, и др.
Опубликовано: (2019)