Familial forms of diabetes insipidus: clinical and molecular characteristics (Q37897472)

25 August 2017

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title

Familial forms of diabetes insipidus: clinical and molecular characteristics (English)

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25 August 2017

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Muriel Babey

1

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25 August 2017

Peter Kopp

series ordinal

2

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25 August 2017

Gary L Robertson

series ordinal

3

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25 August 2017

publication date

5 July 2011

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Nature Reviews Endocrinology

25 August 2017

published in

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25 August 2017

volume

7

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25 August 2017

issue

12

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25 August 2017

page(s)

701-714

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https://scigraph.springernature.com/pub.10.1038/nrendo.2011.100

25 August 2017

exact match

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cites work

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Three families with autosomal dominant nephrogenic diabetes insipidus caused by aquaporin-2 mutations in the C-terminus.

21 January 2018

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An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex

21 January 2018

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Familial neurohypophyseal diabetes insipidus associated with a signal peptide mutation

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Biochemical basis of partial nephrogenic diabetes insipidus phenotypes

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Identification of 13 new mutations in the vasopressin-neurophysin II gene in 17 kindreds with familial autosomal dominant neurohypophyseal diabetes insipidus

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HEREDITARY DIABETES INSIPIDUS

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12 December 2020

Identifiers

DOI

10.1038/NRENDO.2011.100

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25 August 2017

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