Mutation spectrum of Kallmann syndrome: identification of five novel mutations across ANOS1 and FGFR1
Abstract Background Kallmann syndrome (KS) is a common type of idiopathic hypogonadotropic hypogonadism. To date, more than 30 genes including ANOS1 and FGFR1 have been identified in different genetic models of KS without affirmatory genotype–phenotype correlation, and novel mutations have been foun...
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| Principais autores: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMC
2023-03-01
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| coleção: | Reproductive Biology and Endocrinology |
| Assuntos: | |
| Acesso em linha: | https://doi.org/10.1186/s12958-023-01074-w |
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