AB132. The KAL1 pVal610Ile mutation is a recessive mutation causing Kallmann syndrome
@article{TAU4563, author = {Shilin Zhang and Hao Xu and Tao Wang and Guoqing Liu and Jihong Liu}, title = {AB132. The KAL1 pVal610Ile mutation is a recessive mutation causing Kallmann syndrome}, journal = {Translational Andrology and Urology}, volume = {3}, number = {Suppl 1}, year = {2014}, keywords = {}, abstract = {}, issn = {2223-4691}, url = {https://tau.amegroups.org/article/view/4563} }