Brief report: congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene.
Details
Serval ID
serval:BIB_46304710155A
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Brief report: congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene.
Journal
The New England journal of medicine
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
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
Pubmed
Web of science
Create date
30/12/2020 16:44
Last modification date
31/12/2020 7:26