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Volumn 67, Issue 10, 2010, Pages 1252-1256

Association of plastin 3 expression with disease severity in spinal muscular atrophy only in postpubertal females

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN BINDING PROTEIN; MESSENGER RNA; PLASTIN 3; SURVIVAL MOTOR NEURON PROTEIN 2; UNCLASSIFIED DRUG;

EID: 77957939276     PISSN: 00039942     EISSN: 15383687     Source Type: Journal    
DOI: 10.1001/archneurol.2010.239     Document Type: Article
Times cited : (55)

References (11)
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  • 2
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    • Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: Evidence of homozygous deletions of the SMN gene in unaffected individuals
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  • 3
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    • Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy
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    • Cobben, J.M.1    Van Der Steege, G.2    Grootscholten, P.3    De Visser, M.4    Scheffer, H.5    Buys, C.H.6
  • 4
    • 0030051493 scopus 로고    scopus 로고
    • Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy
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  • 5
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    • Homozygous SMN1 deletions in unaffected family members and modification of the phenotype by SMN2
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  • 6
    • 42549088649 scopus 로고    scopus 로고
    • Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy
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  • 7
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    • Plastins: Versatile modulators of actin organization in (patho)physiological cellular processes
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  • 8
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    • The gross motor function measure is a valid and sensitive outcome measure for spinal muscular atrophy
    • AmSMART Group
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.