Detection of compound heterozygous deletions in the parkin gene of fibroblasts in patients with autosomal recessive hereditary parkinsonism (PARK2)

Neuroscience Letters

Volumn 400, Issue 1-2, 2006, Pages 44-47

  Nakaso, Kazuhiro ^a   Adachi, Yoshiki ^a   Yasui, Kenichi ^a   Sakuma, Kenji ^a   Nakashima, Kenji ^a  

^a TOTTORI UNIVERSITY   (Japan)

Author keywords

Compound heterozygous mutation; Fibroblast; Parkin

Indexed keywords

PARKIN;

ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CELLULAR DISTRIBUTION; CLINICAL FEATURE; DELETION MUTANT; DISEASE COURSE; EXON; FEMALE; GENE; GENE AMPLIFICATION; GENE DELETION; GENE MUTATION; GENETIC ANALYSIS; HETEROZYGOTE; HUMAN; IMMUNOBLOTTING; LYMPHOCYTE; MALE; MUSCLE RIGIDITY; ONSET AGE; PARKIN GENE; PARKINSONISM; PRIORITY JOURNAL; PROTEIN EXPRESSION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA ISOLATION; SKIN FIBROBLAST; TREMOR;

DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; FIBROBLASTS; GENE DELETION; HETEROZYGOTE; HUMANS; MALE; PARKINSONIAN DISORDERS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER; UBIQUITIN-PROTEIN LIGASES;

EID: 33646138464     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2006.02.035     Document Type: Article

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