Familial Parkinsonism with digenic Parkin and PINK1 mutations

Movement Disorders

Volumn 23, Issue 10, 2008, Pages 1461-1465

  Funayama, Manabu ^a   Li, Yuanzhe ^a   Tsoi, Tak Hong ^b   Lam, Ching Wan ^c   Ohi, Takekazu ^d   Yazawa, Shogo ^e   Uyama, Eiichiro ^f   Djaldetti, Ruth ^g,j   Melamed, Eldad ^g,j   Yoshino, Hiroyo ^a   Imamichi, Yoko ^a   Takashima, Hiroshi ^h   Nishioka, Kenya ^a   Sato, Kenichi ⁱ   Tomiyama, Hiroyuki ^a   Kubo, Shin Ichiro ^a   Mizuno, Yoshikuni ^a   Hattori, Nobutaka ^a  

^a JUNTENDO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b PAMELA YOUDE NETHERSOLE EASTERN HOSPITAL   (Hong Kong)

^c CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

^d KURASHIKI CENTRAL HOSPITAL   (Japan)

^e Nobeoka Prefectural Hospital   (Japan)

^f KUMAMOTO UNIVERSITY   (Japan)

^g RABIN MEDICAL CENTER   (Israel)

^h KAGOSHIMA UNIVERSITY   (Japan)

ⁱ JUNTENDO UNIVERSITY   (Japan)

^j TEL AVIV UNIVERSITY   (Israel)

more..

Author keywords

Digenic; Parkin; Parkinson's disease; PINK1; Psychiatric disorder

Indexed keywords

PARKIN; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE INDUCED PUTATIVE KINASE 1; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE COURSE; FAMILIAL PARKINSONISM; FEMALE; GENE IDENTIFICATION; GENE INTERACTION; GENE MUTATION; GENETIC ANALYSIS; GENETIC CORRELATION; GENOTYPE; HETEROZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MENTAL DISEASE; ONSET AGE; PARKINSONISM; PRIORITY JOURNAL; SCHIZOPHRENIA; SIBLING;

EID: 52649172321     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.22143     Document Type: Article

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