Non-Classical 21-Hydroxylase Deficiency: Analysis of a Mutant Gene in a Uyghur Family and Literature Review

OBJECTIVE: The gene mutation and clinical characteristics of a patient with non-classical 21-hydroxylase deficiency and his family were analyzed. METHODS: A patient was diagnosed with non-classical 21-hydroxylase deficiency in the Department of Endocrinology of People’s Hospital of Xinjiang Uygur Au...

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Detalles Bibliográficos
Autores principales: Maimaitiming, Jimilanmu, Amuti, Guli, TuHuTi, AiHeMaiTiJiang, Chen, Yuan, Song, Xiang-Xin, Wang, Jing, Alimu, Adila, Zhang, Kaidi, Abudounaiyimu, Munila, Jiang, Jun, Wang, Xin-Ling, Guo, Yan-Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8039199/
https://www.ncbi.nlm.nih.gov/pubmed/33854360
http://dx.doi.org/10.2147/PGPM.S297607

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8039199/
https://www.ncbi.nlm.nih.gov/pubmed/33854360
http://dx.doi.org/10.2147/PGPM.S297607

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