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}
}