A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus.-Reference-Cited by-同舟云学术

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A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus.

Published:1992-01 Issue:1 Volume:11 Page:19-23
ISSN:0261-4189
Container-title:The EMBO Journal
language:en
Short-container-title:The EMBO Journal

Author:

Bahnsen U.,Oosting P.,Swaab D.F.,Nahke P.,Richter D.,Schmale H.

Publisher

Wiley

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/j.1460-2075.1992.tb05022.x/fullpdf

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4. Functional analyses of three different mutations in the AVP-NPII gene causing familial neurohypophyseal diabetes insipidus;Endocrine;2021-07-07

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