Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome: 20 Years After the Identification of the Firstgata3Mutations

AuthID
 P-00S-AVE
2
Author(s)
Thakker, RV
Tipo de Documento
Article
Year published
2020
Publicado
in HUMAN MUTATION, ISSN: 1059-7794
Volume: 41, Número: 8, Páginas: 1341-1350 (10)
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Scopus®
Crossref®23
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 32442337
SCOPUS: 2-s2.0-85086272289
Wos: WOS:000539473500001
Source Identifiers
ISSN: 1059-7794
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