WDR43 c.409G>A ;(p.D137N)

Variant ID: 2-29129371-G-A

NM_015131.1(WDR43):c.409G>A;(p.D137N)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Germline recessive mutations in PI4KA are associated with perisylvian polymicrogyria, cerebellar hypoplasia and arthrogryposis.

Human Molecular Genetics
Pagnamenta, Alistair T AT; Howard, Malcolm F MF; Wisniewski, Eva E; Popitsch, Niko N; Knight, Samantha J L SJ; Keays, David A DA; Quaghebeur, Gerardine G; Cox, Helen H; Cox, Phillip P; Balla, Tamas T; Taylor, Jenny C JC; Kini, Usha U
Publication Date: 2015-07-01

Variant appearance in text: WDR43: 409G>A; D137N
PubMed Link: 25855803
Variant Present in the following documents:
  • supp_ddv117_ddv117supp_table2.xls, sheet 1
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