Clinical Features Associated with Ctnnb1 de Novo Loss of Function Mutations in Ten Individuals

AuthID
 P-00Y-DR4
14
Author(s)
Kharbanda, M
·
Pilz, DT
·
Tomkins, S
·
Chandler, K
·
Saggar, A
·
Fryer, A
·
McKay, V
·
Smith, JC
·
Burn, J
·
Kini, U
·
FitzPatrick, DR
·
Document Type
Article
Year published
2017
Published
in EUROPEAN JOURNAL OF MEDICAL GENETICS, ISSN: 1769-7212
Volume: 60, Issue: 2, Pages: 130-135 (6)
Indexing
Wos®
Scopus®
Crossref®35
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 27915094
Scopus: 2-s2.0-85007545392
Wos: WOS:000398068300008
Source Identifiers
ISSN: 1769-7212
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