Familial neurohypophyseal diabetes insipidus associated with a signal peptide mutation.-Reference-Cited by-同舟云学术

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Familial neurohypophyseal diabetes insipidus associated with a signal peptide mutation.

Published:1993-09 Issue:3 Volume:77 Page:599A-599G
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

McLeod J F,Kovács L,Gaskill M B,Rittig S,Bradley G S,Robertson G L

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/77/3/599A/10503935/jcem599A.pdf

Cited by 88 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. A case of central diabetes insipidus due to neurophysin II gene abnormality diagnosed based on a family history of nocturnal enuresis;Endocrine Journal;2022

2. The Hypothalamus;The Pituitary;2022

3. Diabetes insipidus;La Presse Médicale;2021-12

4. Familial DI and Genetic Workup;Diabetes Insipidus in Children;2021

5. Diabetes insípida central familiar;Medicina Clínica;2020-12

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