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Publications
SEMA3A, a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome
Publication with shared reference
10.1371/journal.pgen.1002896
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Publications
SEMA3A, a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome
Publication with shared reference
10.1371/journal.pgen.1002896
Publications with shared reference:
SEMA3A, a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome
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