Pendred's syndrome and genetic defects in thyroid hormone synthesis.

Détails

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ID Serval
serval:BIB_A840BF8EFE1B
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Production externe
Titre
Pendred's syndrome and genetic defects in thyroid hormone synthesis.
Périodique
Reviews in endocrine & metabolic disorders
Auteur⸱e⸱s
Kopp P.
ISSN
1389-9155 (Print)
ISSN-L
1389-9155
Statut éditorial
Publié
Date de publication
01/2000
Peer-reviewed
Oui
Volume
1
Numéro
1-2
Pages
109-121
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't ; Review
Publication Status: ppublish
Mots-clé
Carrier Proteins/genetics, Carrier Proteins/physiology, Deafness/complications, Deafness/genetics, Goiter/complications, Goiter/genetics, Humans, Hypothyroidism/complications, Hypothyroidism/genetics, Membrane Transport Proteins, Mutation, Perchlorates, Sodium Compounds, Sulfate Transporters, Syndrome, Thyroid Hormones/biosynthesis, Thyroid Hormones/genetics
DOI
10.1023/a:1010024722595
Pubmed
11704986
Création de la notice
30/12/2020 16:11
Dernière modification de la notice
31/12/2020 7:26
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