Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: Cofirmation in 2 kindreds

Archives of Neurology

Volumn 62, Issue 4, 2005, Pages 597-600

  Chen, Dong Hui ^a   Matsushita, Mark ^a   Rainier, Shirley ^c   Meaney, Brandon ^d   Tisch, Lisa ^a   Feleke, Abreham ^a   Wolff, John ^a   Lipe, Hillary ^a   Fink, John ^b,c   Bird, Thomas D ^a,b   Raskind, Wendy H ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

^b VETERANS AFFAIRS MEDICAL CENTER   (United States)

^c UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^d MCMASTER UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; VALINE;

AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 2; CONTROLLED STUDY; DNA SEQUENCE; DYSKINESIA; EXON; FAMILY; FAMILY HISTORY; GENE; GENE FUNCTION; GENE IDENTIFICATION; GENE MAPPING; GENE MUTATION; GENETIC ANALYSIS; GENETIC HETEROGENEITY; HAPLOTYPE; HUMAN; HUMAN CELL; MISSENSE MUTATION; MR1 GENE; NUCLEOTIDE SEQUENCE; PAROXYSMAL NONKINESIGENIC DYSKINESIA; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

ALANINE; AMINO ACID SUBSTITUTION; CHOREATIC DISORDERS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 2; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; GENES, DOMINANT; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; HAPLOTYPES; HUMANS; MALE; MUSCLE PROTEINS; MUTATION, MISSENSE; PEDIGREE; PROTEIN STRUCTURE, SECONDARY; VALINE;

EID: 20144389932     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.62.4.597     Document Type: Article

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