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Publication Detail
SEMA3A, a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome
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Publication Type:Journal article
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Publication Sub Type:Article
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Authors:Hanchate NK, Giacobini P, Lhuillier P, Parkash J, Espy C, Fouveaut C, Leroy C, Baron S, Campagne C, Vanacker C, Collier F, Cruaud C, Meyer V, Garcia-Pinero A, Dewailly D, Cortet-Rudelli C, Gersak K, Metz C, Chabrier G, Pugeat M, Young J, Hardelin J-P, Prevot V, Dode C
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Publisher:PUBLIC LIBRARY SCIENCE
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Publication date:01/08/2012
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Journal:PLOS GENETICS
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Volume:8
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Issue:8
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Article number:ARTN e1002896
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Status:Published
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Print ISSN:1553-7404
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Language:English
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Keywords:Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, GONADOTROPIN-RELEASING-HORMONE, IDIOPATHIC HYPOGONADOTROPIC HYPOGONADISM, OLFACTORY AXONS, SEMAPHORIN-III, NEURONS, MIGRATION, MUTATIONS, MICE, PROTEIN, NERVE
Abstract
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