Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients. [electronic resource]
- European journal of endocrinology Dec 2013
- 805-9 p. digital
Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
1479-683X
10.1530/EJE-13-0419 doi
Adult Africa, Northern Aged Arabs--genetics Europe Exons Extracellular Matrix Proteins--genetics Female Fibroblast Growth Factor 8--genetics Gastrointestinal Hormones--genetics Gene Frequency Humans Introns Kallmann Syndrome--epidemiology Male Middle Aged Mutation Nerve Tissue Proteins--genetics Neuropeptides--genetics Prevalence Receptor, Fibroblast Growth Factor, Type 1--genetics Receptors, G-Protein-Coupled--genetics Receptors, Peptide--genetics Sequence Analysis, DNA White People--genetics