Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia

N. Philip, B. Chabrol, A. M. Lossi, C. Cardoso, R. Guerrini, W. B. Dobyns, C. Raybaud, L. Villard

Research output: Contribution to journalArticlepeer-review

95 Scopus citations
Original languageEnglish (US)
Pages (from-to)441-446
Number of pages6
JournalJournal of medical genetics
Issue number6
StatePublished - Jun 1 2003
Externally publishedYes

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