Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a mutation in the arginine-vasopressin II gene in four generations of a Korean family-Reference-Cited by-同舟云学术

Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a mutation in the arginine-vasopressin II gene in four generations of a Korean family

Published:2014 Issue:4 Volume:19 Page:220
ISSN:2287-1012
Container-title:Annals of Pediatric Endocrinology & Metabolism
language:en
Short-container-title:Ann Pediatr Endocrinol Metab

Author:

Kim Myo-Jing¹,Kim Young-Eun²,Ki Chang-Seok²,Yoo Jae-Ho¹

Affiliation:

1. Department of Pediatrics, Dong-A University College of Medicine, Busan, Korea.

2. Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Publisher

Korean Society of Pediatric Endocrinology

Subject

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

Link

http://e-apem.org/upload/pdf/apem-19-220.pdf

Reference16 articles.

1. Familial neurohypophyseal diabetes insipidus due to a novel mutation in the arginine vasopressin–neurophysin II gene

2. Autosomal recessive familial neurohypophyseal diabetes insipidus: onset in early infancy

3. Diabetes insipidus

4. Radioimmunoassay of vasopressin in familial central diabetes insipidus

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