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Volumn 36, Issue 4, 2015, Pages 1767.e3-1767.e6

CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients

(87)  Chiò, Adriano a,b   Mora, Gabriele c   Sabatelli, Mario d   Caponnetto, Claudia e   Traynor, Bryan J f   Johnson, Janel O f   Nalls, Mike A f   Calvo, Andrea a,b   Moglia, Cristina a   Borghero, Giuseppe g   Monsurrò, Maria Rosaria h   La Bella, Vincenzo i   Volanti, Paolo c   Simone, Isabella j   Salvi, Fabrizio k   Logullo, Francesco O l   Nilo, Riva m   Battistini, Stefania n   Mandrioli, Jessica o   Tanel, Raffaella p   more..

c IRCCS   (Italy)

Author keywords

Amyotrophic lateral sclerosis; CHCHD10; Familial; Sporadic

Indexed keywords

CYTOSINE; PROLINE; SERINE; THYMINE; CHCHD10 PROTEIN, HUMAN; MITOCHONDRIAL PROTEIN;

EID: 84925343216     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2015.01.017     Document Type: Article
Times cited : (47)

References (9)
  • 2
    • 0034574407 scopus 로고    scopus 로고
    • El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis
    • World Federation of Neurology Research Group on Motor Neuron Diseases
    • Brooks B.R., Miller R.G., Swash M., Munsat T.L. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph. Lateral Scler. Other Motor Neuron Disord. 2000, 1:293-299. World Federation of Neurology Research Group on Motor Neuron Diseases.
    • (2000) Amyotroph. Lateral Scler. Other Motor Neuron Disord. , vol.1 , pp. 293-299
    • Brooks, B.R.1    Miller, R.G.2    Swash, M.3    Munsat, T.L.4
  • 8
    • 84893649256 scopus 로고    scopus 로고
    • State of play in amyotrophic lateral sclerosis genetics
    • Renton A.E., Chiò A., Traynor B.J. State of play in amyotrophic lateral sclerosis genetics. Nat Neurosci 2014, 17:17-23.
    • (2014) Nat Neurosci , vol.17 , pp. 17-23
    • Renton, A.E.1    Chiò, A.2    Traynor, B.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.