SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome
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Author / Creator
Hanchate, Naresh Kumar , Giacobini, Paolo , Lhuillier, Pierre , Parkash, Jyoti , Espy, Cécile , Fouveaut, Corinne , Leroy, Chrystel , Baron, Stéphanie , Campagne, Céline , Vanacker, Charlotte , Collier, Francis , Cruaud, Corinne , Meyer, Vincent , García-Piñero, Alfons , Dewailly, Didier , Cortet-Rudelli, Christine , Gersak, Ksenija , Metz, Chantal , Chabrier, Gérard , Pugeat, Michel , Young, Jacques , Hardelin, Jean-Pierre , Prevot, Vincent and Dodé, Catherine
Publisher
United States: Public Library of Science
Journal title
Language
English
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Publisher
United States: Public Library of Science
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Scope and Contents
Contents
Kallmann syndrome (KS) associates congenital hypogonadism due to gonadotropin-releasing hormone (GnRH) deficiency and anosmia. The genetics of KS involves various modes of transmission, including oligogenic inheritance. Here, we report that Nrp1(sema/sema) mutant mice that lack a functional semaphorin-binding domain in neuropilin-1, an obligatory c...
Alternative Titles
Full title
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome
Authors, Artists and Contributors
Author / Creator
Giacobini, Paolo
Lhuillier, Pierre
Parkash, Jyoti
Espy, Cécile
Fouveaut, Corinne
Leroy, Chrystel
Baron, Stéphanie
Campagne, Céline
Vanacker, Charlotte
Collier, Francis
Cruaud, Corinne
Meyer, Vincent
García-Piñero, Alfons
Dewailly, Didier
Cortet-Rudelli, Christine
Gersak, Ksenija
Metz, Chantal
Chabrier, Gérard
Pugeat, Michel
Young, Jacques
Hardelin, Jean-Pierre
Prevot, Vincent
Dodé, Catherine
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_plos_journals_1313507520
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1313507520
Other Identifiers
ISSN
1553-7404,1553-7390
E-ISSN
1553-7404
DOI
10.1371/journal.pgen.1002896
