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Article

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

European journal of endocrinology - 1 Dec 2013

Sarfati Julie, Fouveaut Corinne, Leroy Chrystel, Jeanpierre Marc, Hardelin Jean-Pierre, Dodé Catherine

Abstract excerpt

CONTEXT: Kallmann syndrome (KS) is a genetically heterogeneous developmental disorder that associates hypogonadotropic hypogonadism and anosmia. Various causative genes have been identified, but their respective involvement in different world regions is poorly documented. OBJECTIVE: We aimed to compare the prevalence of mutations in five routinely analyzed KS genes between Maghrebian and European patients....

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Source

Identifiers

PMID: 24031091
DOI: 10.1530/EJE-13-0419

Genes

PROKR2
FGF8
FGFR1
PROK2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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