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Volumn 138, Issue 8, 2015, Pages e372-

CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA; MITOCHONDRIAL PROTEIN;

EID: 84938857563     PISSN: 00068950     EISSN: 14602156     Source Type: Journal    
DOI: 10.1093/brain/awu384     Document Type: Letter
Times cited : (64)

References (14)
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  • 2
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  • 3
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    • Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients
    • Chaussenot A, Le Ber I, Ait-El-Mkadem S, Camuzat A, de Septenville A, Bannwarth S, et al. Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients. Neurobiol Aging 2014; 35: 2884.e1-4.
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  • 5
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    • Mitochondrial respiratory chain dysfunction in muscle from patients with amyotrophic lateral sclerosis
    • Crugnola V, Lamperti C, Lucchini V, Ronchi D, Peverelli L, Prelle A, et al. Mitochondrial respiratory chain dysfunction in muscle from patients with amyotrophic lateral sclerosis. Arch Neurol 2010; 67: 849-54.
    • (2010) Arch Neurol , vol.67 , pp. 849-854
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  • 6
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    • The mitochondrial disulfide relay system protein GFER is mutated in autosomal-recessive myopathy with cataract and combined respiratory-chain deficiency
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    • Di Fonzo, A.1    Ronchi, D.2    Lodi, T.3    Fassone, E.4    Tigano, M.5    Lamperti, C.6
  • 9
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.