Mutations in the Pendred Syndrome (PDS/SLC26A) gene: an increasingly complex phenotypic spectrum from goiter to thyroid hypoplasia.
Détails
ID Serval
serval:BIB_A91022C93CF9
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Mutations in the Pendred Syndrome (PDS/SLC26A) gene: an increasingly complex phenotypic spectrum from goiter to thyroid hypoplasia.
Périodique
The Journal of clinical endocrinology and metabolism
ISSN
1945-7197 (Electronic)
ISSN-L
0021-972X
Statut éditorial
Publié
Date de publication
01/2014
Peer-reviewed
Oui
Volume
99
Numéro
1
Pages
67-69
Langue
anglais
Notes
Publication types: Editorial ; Comment
Publication Status: ppublish
Publication Status: ppublish
Mots-clé
Congenital Hypothyroidism/genetics, Female, Humans, Male, Membrane Transport Proteins/genetics, Sulfate Transporters, Thyroid Dysgenesis/genetics
Pubmed
Web of science
Open Access
Oui
Création de la notice
27/12/2020 23:46
Dernière modification de la notice
28/12/2020 7:26
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