Brief report: congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene.
Détails
ID Serval
serval:BIB_46304710155A
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Brief report: congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene.
Périodique
The New England journal of medicine
ISSN
0028-4793 (Print)
ISSN-L
0028-4793
Statut éditorial
Publié
Date de publication
19/01/1995
Peer-reviewed
Oui
Volume
332
Numéro
3
Pages
150-154
Langue
anglais
Notes
Publication types: Case Reports ; Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
Publication Status: ppublish
Publication Status: ppublish
Mots-clé
Amino Acid Sequence, Child, DNA Fingerprinting, Germ-Line Mutation, Humans, Hyperthyroidism/congenital, Hyperthyroidism/genetics, Infant, Newborn, Male, Molecular Sequence Data, Receptors, Thyrotropin/genetics, Transfection
Pubmed
Web of science
Création de la notice
30/12/2020 16:44
Dernière modification de la notice
31/12/2020 7:26