Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's disease

NeuroReport

Volumn 10, Issue 2, 1999, Pages 427-429

  Lincoln, Sarah ^a   Vaughan, Jenny ^b   Wood, Nick ^b   Baker, Matt ^a   Adamson, Jennifer ^a   Gwinn Hardy, Katrina ^a   Lynch, Tim ^c   Hardy, John ^a   Farrer, Matt ^a  

^a MAYO CLINIC   (United States)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c MATER MISERICORDIAE UNIVERSITY HOSPITAL   (Ireland)

Author keywords

Genetics; Parkinson's disease; Ubiquitin carboxy terminal hydrolase L1

Indexed keywords

OXYGENASE;

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; DNA POLYMORPHISM; GENE MUTATION; GENE SEQUENCE; GENETIC TRANSCRIPTION; HUMAN; MAJOR CLINICAL STUDY; NUCLEIC ACID BASE SUBSTITUTION; PARKINSON DISEASE; PRIORITY JOURNAL;

EID: 0033525009     PISSN: 09594965     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001756-199902050-00040     Document Type: Article

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