Kallmann syndrome with a Tyr113His PROKR2 mutation-Reference-Cited by-同舟云学术

Kallmann syndrome with a Tyr113His PROKR2 mutation

Published:2017-09 Issue:35 Volume:96 Page:e7974
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Ha Jeong-Ha,Lee Sara,Kim Youngmoon,Moon Ji In,Seo Jongkwon,Jang Ja-Hyun,Cho Eun-Hae,Kim Jung Min,Rhee Byoung Doo,Ko Kyung Soo,Yoo Soo Jin,Won Jong Chul

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

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5. Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum;Cole;J Clin Endocrinol Metab,2008

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