R G Korneluk, M A Narang. Show Affiliations »
Abstract
Mesh: See more » AnimalsFemaleFragile X Syndrome/geneticsHumansHuntington Disease/geneticsMaleMiceMice, KnockoutMice, TransgenicMyotonic Dystrophy/geneticsSpinocerebellar Degenerations/geneticsTrinucleotide Repeats
Year: 1997 PMID: 9020832 DOI: 10.1038/ng0297-119
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330