A new F-box protein 7 gene mutation causing typical Parkinson's disease

Movement Disorders

Volumn 30, Issue 8, 2015, Pages 1130-1133

  Lohmann, Ebba ^a,b   Coquel, Anne Sophie ^c,d,e,f   Honoré, Aurélie ^c,d,e,f   Gurvit, Hakan ^a   Hanagasi, Hasmet ^a   Emre, Murat ^a   Leutenegger, Anne L ^d,g   Drouet, Valérie ^c,d,e,f   Sahbatou, Mourad ^h   Guven, Gamze ⁱ   Erginel Unaltuna, Nihan ⁱ   Deleuze, Jean Francois ^j   Lesage, Suzanne ^c,d,e,f   Brice, Alexis ^c,d,e,f,k  

^a ISTANBUL UNIVERSITY   (Turkey)

^b UNIVERSITY OF TÜBINGEN   (Germany)

^c SORBONNE UNIVERSITÉ   (France)

^d INSERM   (France)

^e CNRS   (France)

^f ICM   (France)

^g UNIVERSITÉ PARIS DIDEROT   (France)

^h FONDATION JEAN DAUSSET CEPH   (France)

ⁱ ISTANBUL UNIVERSITY   (Turkey)

^j CENTRE NATIONAL DE GÉNOTYPAGE   (France)

^k PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

more..

Author keywords

autosomal recessive; FBXO7 gene; Parkinson disease; phenotype; Turkey

Indexed keywords

F BOX PROTEIN; FBXO7 PROTEIN, HUMAN;

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; EXOME; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC VARIATION; HUMAN; MALE; PARKINSON DISEASE; PHENOTYPE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; TURKEY (REPUBLIC); CASE REPORT; CONSANGUINITY; GENETICS; MIDDLE AGED; MUTATION; PATHOPHYSIOLOGY; PEDIGREE; TURKEY; VERY ELDERLY;

AGED, 80 AND OVER; CONSANGUINITY; F-BOX PROTEINS; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION; PARKINSON DISEASE; PEDIGREE; TURKEY;

EID: 84929773699     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.26266     Document Type: Article

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