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A novel nonsense mutation of the KAL1 gene (p.Trp204*) in Kallmann syndrome
OBJECTIVE: To describe a novel KAL1 mutation in patients affected by Kallmann syndrome. SETTING: Endocrinology Clinic of the João de Barros Barreto University Hospital – Federal University of Pará, Brazil. METHODS: Clinical examination, hormone assays and sequencing of exons 5, 6 and 9 of the KAL1 g...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196791/ https://www.ncbi.nlm.nih.gov/pubmed/25328414 http://dx.doi.org/10.2147/TACG.S64280 |