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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Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Int J Endocrinol
Päätekijät: Marzuki, Nanis S., Idris, Firman P., Kartapradja, Hannie D., Harahap, Alida R., Batubara, Jose R. L.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Hindawi 2019
Aiheet:
Research Article
Linkit: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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