Mutations in the Pendred Syndrome (PDS/SLC26A) gene: an increasingly complex phenotypic spectrum from goiter to thyroid hypoplasia.

Details

Serval ID
serval:BIB_A91022C93CF9
Type
Article: article from journal or magazin.
Collection
Publications
Title
Mutations in the Pendred Syndrome (PDS/SLC26A) gene: an increasingly complex phenotypic spectrum from goiter to thyroid hypoplasia.
Journal
The Journal of clinical endocrinology and metabolism
Author(s)
Kopp P.
ISSN
1945-7197 (Electronic)
ISSN-L
0021-972X
Publication state
Published
Issued date
01/2014
Peer-reviewed
Oui
Volume
99
Number
1
Pages
67-69
Language
english
Notes
Publication types: Editorial ; Comment
Publication Status: ppublish
Keywords
Congenital Hypothyroidism/genetics, Female, Humans, Male, Membrane Transport Proteins/genetics, Sulfate Transporters, Thyroid Dysgenesis/genetics
Pubmed
Web of science
Open Access
Yes
Create date
27/12/2020 22:46
Last modification date
28/12/2020 6:26
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