Characterising SRD5A2 Gene Variants in 37 Indonesian Patients with 5-Alpha-Reductase Type 2 Deficiency

The 5-alpha-reductase type 2 deficiency (5ARD2) is an autosomal recessive condition associated with impairment in the conversion of testosterone to dihydrotestosterone. This condition leads to undervirilisation in 46,XY individuals. To date, there have been more than 100 variations identified in the...

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Detalhes bibliográficos
Publicado no:Int J Endocrinol
Main Authors: Marzuki, Nanis S., Idris, Firman P., Kartapradja, Hannie D., Harahap, Alida R., Batubara, Jose R. L.
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi 2019
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6914983/
https://ncbi.nlm.nih.gov/pubmed/31885560
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2019/7676341
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