Brief report: congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene.

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Serval ID
serval:BIB_46304710155A
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Production externe
Title
Brief report: congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene.
Journal
The New England journal of medicine
Author(s)
Kopp P., van Sande J., Parma J., Duprez L., Gerber H., Joss E., Jameson J.L., Dumont J.E., Vassart G.
ISSN
0028-4793 (Print)
ISSN-L
0028-4793
Publication state
Published
Issued date
19/01/1995
Peer-reviewed
Oui
Volume
332
Number
3
Pages
150-154
Language
english
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
Keywords
Amino Acid Sequence, Child, DNA Fingerprinting, Germ-Line Mutation, Humans, Hyperthyroidism/congenital, Hyperthyroidism/genetics, Infant, Newborn, Male, Molecular Sequence Data, Receptors, Thyrotropin/genetics, Transfection
DOI
10.1056/NEJM199501193320304
Pubmed
7800007
Web of science
A1995QB16000004
Create date
30/12/2020 16:44
Last modification date
31/12/2020 7:26
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