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Prevalence of CYP17A1 gene mutations in 17α-hydroxylase deficiency in the Chinese Han population
BACKGROUND: 17α-hydroxylase deficiency is a rare autosomal recessive disorder caused by mutations in the cytochrome P450 family 17 subfamily A member 1 gene. The major clinical presentation includes hypertension, hypokalemia, male pseudohermaphroditism and female gonadal dysplasia. Hundreds of patho...
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| Publicado en: | Clin Hypertens |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6792268/ https://ncbi.nlm.nih.gov/pubmed/31636948 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40885-019-0128-6 |
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