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Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland
BACKGROUND: Kallmann syndrome (KS), comprised of congenital hypogonadotropic hypogonadism (HH) and anosmia, is a clinically and genetically heterogeneous disorder. Its exact incidence is currently unknown, and a mutation in one of the identified KS genes has only been found in ~30% of the patients....
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2011
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3143089/ https://ncbi.nlm.nih.gov/pubmed/21682876 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-6-41 |
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