Functional analysis of SEMA3A variants identified in Chinese patients with isolated hypogonadotropic hypogonadism-Reference-Cited by-同舟云学术

Functional analysis of SEMA3A variants identified in Chinese patients with isolated hypogonadotropic hypogonadism

Author:

Dai Wenting¹²³^ORCID,Li Jia‐Da¹²³,Zhao Yaguang¹²³,Wu Jiayu¹²³^ORCID,Jiang Fang¹²³,Chen Dan‐Na⁴,Zheng Ruizhi⁵,Men Meichao⁶

Affiliation:

1. School of Life SciencesCentral South University Changsha China

2. Hunan Key Laboratory of Animal Models for Human DiseasesCentral South University Changsha China

3. Hunan Key Laboratory of Medical GeneticsCentral South University Changsha China

4. Department of Basic Medical SciencesChangsha Medical University Changsha China

5. Department of Endocrinologythe People's Hospital of Henan Province Zhengzhou China

6. Health Management Center of Xiangya HospitalCentral South University Changsha China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

Reference33 articles.

3. Genetic basis and variable phenotypic expression of Kallmann syndrome: towards a unifying theory;Mitchell AL;Trends Endocrinol Metab,2011

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