Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients.

Sarfati, Julie

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