AFX1 and p54(nrb): Fine mapping, genomic structure, and exclusion as candidate genes of X-linked dystonia parkinsonism

Human Genetics

Volumn 100, Issue 5-6, 1997, Pages 569-572

  Peters, Usha ^a   Haberhausen, Gerd ^a   Kostrzewa, Markus ^a   Nolte, Dagmar ^a   Müller, Ulrich ^a  

^a JUSTUS LIEBIG UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRAIN; CONTROLLED STUDY; DNA FLANKING REGION; DYSTONIA; EXON; GENE MAPPING; GENE STRUCTURE; HUMAN; HUMAN TISSUE; INTRON; MOUSE; NONHUMAN; NORTHERN BLOTTING; PARKINSONISM; PRIORITY JOURNAL; STOP CODON; X CHROMOSOME LINKAGE; YEAST ARTIFICIAL CHROMOSOME; ANIMAL; ANTIBODY SPECIFICITY; CHROMOSOME MAP; DNA SEQUENCE; GENE; GENETIC LINKAGE; GENETICS; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PARKINSON DISEASE; RESTRICTION MAPPING; SYNDROME; X CHROMOSOME;

MESSENGER RNA; MLLT7 PROTEIN, HUMAN; NONO PROTEIN, HUMAN; NUCLEAR MATRIX PROTEIN; NUCLEAR PROTEIN; OCTAMER TRANSCRIPTION FACTOR; RNA BINDING PROTEIN; TRANSCRIPTION FACTOR;

ANIMALS; BASE SEQUENCE; CHROMOSOME MAPPING; DYSTONIA; EXONS; GENES; HUMANS; LINKAGE (GENETICS); MICE; MOLECULAR SEQUENCE DATA; NUCLEAR MATRIX-ASSOCIATED PROTEINS; NUCLEAR PROTEINS; OCTAMER TRANSCRIPTION FACTORS; ORGAN SPECIFICITY; PARKINSON DISEASE; RESTRICTION MAPPING; RNA, MESSENGER; RNA-BINDING PROTEINS; SEQUENCE ANALYSIS, DNA; SYNDROME; TRANSCRIPTION FACTORS; X CHROMOSOME;

EID: 0031429098     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050553     Document Type: Article

References (13)

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