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
Objective:Carboxypeptidase E (CPE) plays a critical role in the biosynthesis of peptide hormones and neuropeptides in the endocrine system and central nervous system. CPE knockout mice models exhibit disorders such as diabetes, hyperproinsulinaemia, low bone mineral density and neurodevelopmental di...
| الحاوية / القاعدة: | JCRPE |
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| المؤلفون الرئيسيون: | , , , , , , , , , |
| التنسيق: | مقال |
| اللغة: | الإنجليزية |
| منشور في: |
Pediatric Endocrinology and Diabetes Society
2021-03-01
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| الموضوعات: | |
| الوصول للمادة أونلاين: |
http://www.jcrpe.org/archives/archive-detail/article-preview/a-new-cause-of-obesity-syndrome-associated-with-a-/40188
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