PS-039 A New Mutation Causing Familial Neurohypophyseal Diabetes Insipidus In A Portuguese Family

S Lopes; A Fernandes; P Tavares; MC Lemos; S Gama de Sousa

doi:10.1136/archdischild-2014-307384.334

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Endocrinology and Metabolism

PS-039 A New Mutation Causing Familial Neurohypophyseal Diabetes Insipidus In A Portuguese Family

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Authors

S Lopes 1Pediatrics Department, Centro Hospitalar Do Médio Ave E. P. E., Vila Nova de Famalicão, Portugal PubMed articles Google scholar articles
A Fernandes 1Pediatrics Department, Centro Hospitalar Do Médio Ave E. P. E., Vila Nova de Famalicão, Portugal PubMed articles Google scholar articles
P Tavares 2CGC Genetics, CGC Genetics, Porto, Portugal PubMed articles Google scholar articles
MC Lemos 3Health Sciences Research Centre (CICS), Faculty of Health Sciences University of Beira Interior, Covilhã, Portugal PubMed articles Google scholar articles
S Gama de Sousa 1Pediatrics Department, Centro Hospitalar Do Médio Ave E. P. E., Vila Nova de Famalicão, Portugal PubMed articles Google scholar articles

Citation

Lopes S, Fernandes A, Tavares P, et al

PS-039 A New Mutation Causing Familial Neurohypophyseal Diabetes Insipidus In A Portuguese Family

Archives of Disease in Childhood 2014;99:A125.

Publication history

First published October 14, 2014.

Online issue publication

July 09, 2018

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