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AB132. The KAL1 pVal610Ile mutation is a recessive mutation causing Kallmann syndrome
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@article{{TAU}{4563}, author = {Zhang, S., Xu, H., Wang, T., Liu, G., Liu, J.}, 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}, url = {https://tau.amegroups.org/article/view/4563} }