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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Detalles Bibliográficos
Autores principales: Marzuki, Nanis S., Idris, Firman P., Kartapradja, Hannie D., Harahap, Alida R., Batubara, Jose R. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6914983/
https://www.ncbi.nlm.nih.gov/pubmed/31885560
http://dx.doi.org/10.1155/2019/7676341

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6914983/
https://www.ncbi.nlm.nih.gov/pubmed/31885560
http://dx.doi.org/10.1155/2019/7676341

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