Mutations in DJ-1 are rare in familial Parkinson disease

Neuroscience Letters

Volumn 408, Issue 3, 2006, Pages 209-213

  Pankratz, Nathan ^a   Pauciulo, Michael W ^b   Elsaesser, Veronika E ^b   Marek, Diane K ^b   Halter, Cheryl A ^a   Wojcieszek, Joanne ^a   Rudolph, Alice ^c   Shults, Clifford W ^d,e   Foroud, Tatiana ^a   Nichols, William C ^b,f  

^a INDIANA UNIVERSITY MEDICAL CENTER   (United States)

^b CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^c UNIVERSITY OF ROCHESTER   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e VA SAN DIEGO HEALTHCARE SYSTEM   (United States)

^f UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

Author keywords

DJ 1; MLPA; Multiplex ligation dependent probe amplification; Parkinson disease

Indexed keywords

ADULT; AGED; ARTICLE; CONTROLLED STUDY; DNA POLYMORPHISM; EXON; GENE; GENE AMPLIFICATION; GENE DELETION; GENE DUPLICATION; GENE LOCUS; GENE MUTATION; GENE PROBE; HETEROZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PARK7 GENE; PARKINSON DISEASE; PRIORITY JOURNAL; SCORING SYSTEM;

AGED; AGED, 80 AND OVER; ARGININE; EXONS; FEMALE; GLUTAMIC ACID; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; LOD SCORE; MALE; MIDDLE AGED; MUTATION; ONCOGENE PROTEINS; PARKINSONIAN DISORDERS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER;

EID: 33749519563     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2006.09.003     Document Type: Article

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