Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia (Q24676883)
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(P577) Sunday, June 1, 2003
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(P1476) "Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia" (language: en)
(P2093) N Philip
B Chabrol
A-M Lossi
C Cardoso
R Guerrini
W B Dobyns
C Raybaud
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