Pendred's syndrome and genetic defects in thyroid hormone synthesis.
Details
Serval ID
serval:BIB_A840BF8EFE1B
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Pendred's syndrome and genetic defects in thyroid hormone synthesis.
Journal
Reviews in endocrine & metabolic disorders
ISSN
1389-9155 (Print)
ISSN-L
1389-9155
Publication state
Published
Issued date
01/2000
Peer-reviewed
Oui
Volume
1
Number
1-2
Pages
109-121
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't ; Review
Publication Status: ppublish
Publication Status: ppublish
Keywords
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
Pubmed
Create date
30/12/2020 16:11
Last modification date
31/12/2020 7:26
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