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Volumn 2, Issue 2, 2001, Pages 93-97

Mutations in the lysyl oxidase gene are not associated with amyotrophic lateral sclerosis

Author keywords

Amyotrophic lateral sclerosis; Copper; Lysyl oxidase gene; Polymorphism; Skin

Indexed keywords

ARGININE; COLLAGEN; COPPER; COPPER ZINC SUPEROXIDE DISMUTASE; ELASTIN; GLYCINE; PROLINE; PROTEIN LYSINE 6 OXIDASE;

EID: 0034811310     PISSN: 14660822     EISSN: None     Source Type: Journal    
DOI: 10.1080/146608201316949532     Document Type: Article
Times cited : (6)

References (31)
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  • 10
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  • 11
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    • An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria
    • (1995) Neuron , vol.14 , pp. 1105-1116
    • Wong, P.C.1    Pardo, C.A.2    Borchelt, D.R.3
  • 26
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    • El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis
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    • Brooks, B.R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.