Abstract
By examining two previously described families with rapid-onset dystonia parkinsonism, we have identified a key recombination event that places the disease locus (DYT12) into a 5.9 cM interval flanked by markers D19S224 and D19S900. Evaluation of a positional candidate gene, the glutamate receptor subunit GRIK5, revealed no mutations.
Copyright 2004 Movement Disorder Society
Publication types
-
Research Support, Non-U.S. Gov't
-
Research Support, U.S. Gov't, P.H.S.
MeSH terms
-
Chromosomes, Human, Pair 19 / genetics*
-
DNA Primers / genetics
-
Dystonia / genetics*
-
Exons / genetics
-
Gene Expression
-
Genetic Linkage
-
Genetic Markers
-
Genotype
-
Humans
-
Introns / genetics
-
Parkinsonian Disorders / genetics*
-
Point Mutation / genetics
-
Polymerase Chain Reaction
-
RNA, Messenger / genetics
-
Receptor, Metabotropic Glutamate 5
-
Receptors, Metabotropic Glutamate / genetics*
Substances
-
DNA Primers
-
Genetic Markers
-
RNA, Messenger
-
Receptor, Metabotropic Glutamate 5
-
Receptors, Metabotropic Glutamate