Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia
- PMID: 12807966
- PMCID: PMC1735502
- DOI: 10.1136/jmg.40.6.441
Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia
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