Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease

Neurology

Volumn 72, Issue 19, 2009, Pages 1669-1676

  Ber, I Le ^a,b   Camuzat, A ^a   Berger, E ^c   Hannequin, D ^e   Laquerriere A ^f   Golfier, V ^g   Seilhean, D ^h   Viennet, G ^d   Couratier, P ⁱ   Verpillar, P ^a   Heath, S ^j   Camu, W ^k   Martinaud, O ^e   Lacomblez, L ^b,l   Vercelletto, M ^m   Salachas, F ^b   Sellal, F ^e   Didic, M ⁿ   Thomas Anterion, C ^o   Puel, M ^p   Michel, B F ^q   Besse, C ^j   Duyckaerts, C ^h,l   Meininger, V ^b   Campion, D ^e   Dubois, B ^b,l   Brice, A ^a,b,l   more..

^a INSTITUT DU CERVEAU ET DE LA MOELLE ÉPINIÈRE   (France)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^c Service de Neurologie

^d UNIVERSITY HOSPITAL OF BESANÇON   (France)

^e INSERM   (France)

^f HÔPITAL CHARLES NICOLLE   (France)

^g RENNES UNIVERSITY HOSPITAL   (France)

^h Laboratoire de Neuropathologie R Es courolle

ⁱ LIMOGES UNIVERSITY HOSPITAL   (France)

^j CENTRE NATIONAL DE GÉNOTYPAGE   (France)

^k GUI DE CHAULIAC HOSPITAL   (France)

^l SORBONNE UNIVERSITÉ   (France)

^m NANTES UNIVERSITY HOSPITAL   (France)

ⁿ TIMONE HOSPITAL   (France)

^o UNIVERSITY HOSPITAL OF SAINT ETIENNE   (France)

^p CHU RANGUEIL   (France)

^q HÔPITAL SAINTE MARGUERITE   (France)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; CHROMOSOME 9P; FAMILIAL DISEASE; FRANCE; FRONTOTEMPORAL DEMENTIA; GENE LOCUS; GENE MUTATION; GENETIC LINKAGE; GENETIC SCREENING; HAPLOTYPE; HUMAN; MARKER GENE; MOTOR NEURON DISEASE; ONSET AGE; PRIORITY JOURNAL;

EID: 67049135828     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e3181a55f1c     Document Type: Article

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