A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogonadism-Reference-Cited by-同舟云学术

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A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogonadism

Published:2021-02-26 Issue:1 Volume:13 Page:52-60
ISSN:1308-5727
Container-title:Journal of Clinical Research in Pediatric Endocrinology
language:
Short-container-title:Jcrpe

Author:

Durmaz Asude^ORCID,Aykut Ayça^ORCID,Atik Tahir^ORCID,Özen Samim^ORCID,Ayyıldız Emecen Durdugül^ORCID,Ata Aysun^ORCID,Işık Esra^ORCID,Gökşen Damla^ORCID,Çoğulu Özgür^ORCID,Özkınay Ferda^ORCID

Publisher

Galenos Yayinevi

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Cited by 24 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Insulin receptor isoform B is required for efficient proinsulin processing in pancreatic β cells;iScience;2024-07

2. The Genetics of Obesity;Pediatric Clinics of North America;2024-07

3. Relevant Aspects of Combined Protocols for Prevention of N(M)AFLD and Other Non‐Communicable Diseases;Molecular Nutrition & Food Research;2024-03-20

4. A Comprehensive Review of Syndromic Forms of Obesity: Genetic Etiology, Clinical Features and Molecular Diagnosis;Current Obesity Reports;2024-01-26

5. Heteropterans: a treasure trove of therapeutic proteins;Journal of Insects as Food and Feed;2024-01-10

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