SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.
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PLoS Genet. 2012 Aug;8(8):e1002896. doi: 10.1371/journal.pgen.1002896. Epub 2012 Aug 23.
PLoS Genet. 2012.
PMID: 22927827
Free PMC article.