SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome
SEMA3A 是一种参与轴突寻路的基因，在患有卡尔曼综合征的患者中发生突变
期刊:PLoS Genetics
影响因子:
doi:10.1371/journal.pgen.1002896
Naresh Kumar Hanchate, Paolo Giacobini, Pierre Lhuillier, Jyoti Parkash, Cécile Espy, Corinne Fouveaut, Chrystel Leroy, Stéphanie Baron, Céline Campagne, Charlotte Vanacker, Francis Collier, Corinne Cruaud, Vincent Meyer, Alfons García-Piñero, Didier Dewailly, Christine Cortet-Rudelli, Ksenija Gersa
