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Volumn 138, Issue 12, 2015, Pages e400-

Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain

(36)  Dols Icardo, Oriol a,b   Nebot, Irene b,c,d   Gorostidi, Ana b,e   Ortega Cubero, Sara b,f   Hernández, Isabel g   Rojas García, Ricard a   García Redondo, Alberto h,i   Povedano, Monica j   Lladó, Albert k   Álvarez, Victoria l   Sánchez Juan, Pascual b,m   Pardo, Julio n   Jericó, Ivonne o   Vázquez Costa, Juan i,p   Sevilla, Teresa i,p   Cardona, Fernando b,c,d   Indakoechea, Begoña b,e,q   Moreno, Fermín b,e,q   Fernández Torrón, Roberto b,e,q   Muñoz Llahuna, Laia a,b   more..


Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; AMYOTROPHIC LATERAL SCLEROSIS; BRADYKINESIA; CHCHD10 GENE; CLINICAL ASSESSMENT; DISEASE COURSE; DISEASE DURATION; DISORIENTATION; EXON; FRONTOTEMPORAL DEMENTIA; GENE; GENE FUNCTION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC CODE; GENETIC SCREENING; GENETIC VARIABILITY; HEREDITY; HUMAN; LANGUAGE DISABILITY; LETTER; MINI MENTAL STATE EXAMINATION; NEUROPSYCHOLOGICAL TEST; NONSENSE MUTATION; ONSET AGE; PARKINSONISM; PHENOTYPE; PRIORITY JOURNAL; PROGRESSIVE NONFLUENT APHASIA; RIGIDITY; SPAIN; STOP CODON; AGED; CASE CONTROL STUDY; COMPLICATION; FEMALE; GENETICS; MALE; MOTOR NEURON DISEASE; MUTATION;

EID: 84951174332     PISSN: 00068950     EISSN: 14602156     Source Type: Journal    
DOI: 10.1093/brain/awv175     Document Type: Letter
Times cited : (55)

References (10)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.