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Article

Mutation screening of SEMA3A and SEMA7A in patients with congenital hypogonadotropic hypogonadism.

Pediatric research - 1 May 2014

Känsäkoski Johanna, Fagerholm Rainer, Laitinen Eeva-Maria, Vaaralahti Kirsi, Hackman Peter, Pitteloud Nelly, Raivio Taneli, Tommiska Johanna

Abstract excerpt

BACKGROUND: Congenital hypogonadotropic hypogonadism (HH), a rare disorder characterized by absent, partial, or delayed puberty, can be caused by the lack or deficient number of hypothalamic gonadotropin-releasing hormone (GnRH) neurons. SEMA3A was recently implicated in the etiology of the disor...

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Source

Identifiers

PMID: 24522099
DOI: 10.1038/pr.2014.23

Genes

FGFR1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24522099-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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