A novel variant luteinizing hormone receptor in the first transmembrane helix of two homozygous Iranian patients: case report
Abstract Background Leydig cell hypoplasia (LCH) is a rare autosomal recessive endocrine syndrome that affects the normal development of male external genitalia in 46, XY individuals and is one of the causes of disorder of sexual differentiation (DSD) in males. The responsible gene of LCH is LHCGR w...
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
SpringerOpen
2022-05-01
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| Col·lecció: | Egyptian Journal of Medical Human Genetics |
| Matèries: | |
| Accés en línia: | https://doi.org/10.1186/s43042-022-00305-w |
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