Exome Sequencing Identifies Inppl1 Mutations as a Cause of Opsismodysplasia

AuthID
 P-002-19M
16
Author(s)
Huber, C
·
Frigo, A
·
Nitschke, P
·
Roume, J
·
Shalev, SA
·
Le Merrer, M
·
Tipo de Documento
Article
Year published
2013
Publicado
in AMERICAN JOURNAL OF HUMAN GENETICS, ISSN: 0002-9297
Volume: 92, Número: 1, Páginas: 144-149 (6)
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Publication Identifiers
Pubmed: 23273569
SCOPUS: 2-s2.0-84872303242
Wos: WOS:000313759000016
Source Identifiers
ISSN: 0002-9297
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