Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism-Reference-Cited by-同舟云学术

Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism

Author:

Kotan Leman D.¹^ORCID,Isik Emregul²,Turan Ihsan¹,Mengen Eda³,Akkus Gamze⁴,Tastan Mehmet¹,Gurbuz Fatih¹,Yuksel Bilgin¹,Topaloglu A. Kemal¹⁵⁶

Affiliation:

1. Division of Pediatric Endocrinology; Cukurova University, Faculty of Medicine; Adana Turkey

2. Gaziantep Children's Hospital, Department of Pediatrics, Clinics of Pediatric Endocrinology; Gaziantep Turkey

3. Department of Pediatrics, Division of Pediatric Endocrinology; Ankara Children's Hematology and Oncology Training Hospital; Ankara Turkey

4. Division of Endocrinology; Cukurova University, Faculty of Medicine; Adana Turkey

5. Department of Pediatrics, Division of Pediatric Endocrinology; University of Mississippi Medical Center; Jackson Mississippi

6. Department of Neurobiology and Anatomical Sciences; University of Mississippi Medical Center; Jackson Mississippi

Funder

Cukurova University

Türkiye Bilimsel ve Teknolojik Araştirma Kurumu

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference22 articles.

3. Update on the genetics of idiopathic hypogonadotropic hypogonadism;Topaloglu;J Clin Res Pediatr Endocrinol,2017

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