Phenotypic and Functional Consequences of Haploinsufficiency of Genes from Exocyst and Retinoic Acid Pathway Due to a Recurrent Microdeletion of 2P13.2

AuthID
P-006-97J
14
Author(s)
Wen, J
·
Lopes, F
·
Soares, G
·
Farrell, SA
·
Nelson, C
·
Qiao, Y
·
Ylstra, B
·
Lewis, S
·
Document Type
Article
Year published
2013
Published
in ORPHANET JOURNAL OF RARE DISEASES, ISSN: 1750-1172
Volume: 8, Issue: 1, Pages: 100 (12)
Indexing
Publication Identifiers
Pubmed: 23837398
Scopus: 2-s2.0-84879999423
Wos: WOS:000321696700001
Source Identifiers
ISSN: 1750-1172
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