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Nat Genet. 2008 Sep;40(9):1113-8. doi: 10.1038/ng.204.

tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia.

Author information

1
Cologne Center for Genomics and Institute for Genetics, University of Cologne, Cologne, Germany.

Abstract

Pontocerebellar hypoplasias (PCH) represent a group of neurodegenerative autosomal recessive disorders with prenatal onset, atrophy or hypoplasia of the cerebellum, hypoplasia of the ventral pons, microcephaly, variable neocortical atrophy and severe mental and motor impairments. In two subtypes, PCH2 and PCH4, we identified mutations in three of the four different subunits of the tRNA-splicing endonuclease complex. Our findings point to RNA processing as a new basic cellular impairment in neurological disorders.

PMID:
18711368
DOI:
10.1038/ng.204
[Indexed for MEDLINE]

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