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High creatine kinase levels and white matter changes: Clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiency

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第一作者： Beytía,M.D.L.A.

作者： Beytía,M.D.L.A. ^[1] ; Dekomien,G. ^[2] ; Hoffjan,S. ; Haug,V. ; Anastasopoulos,C. ; Kirschner,J.

作者单位： Department of Human Genetics, Ruhr-University Bochum, Germany ^[1] Division of Neuropediatrics and Muscle Disorders, University Medical Centre, Freiburg, Germany ^[2]

关键词 Congenital muscular dystrophy Genetics LAMA2 Laminin alpha-2 deficiency Merosin White matter abnormality

发布时间 2014-10-14

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Molecular and Cellular Probes

2014年28卷4期

118-122页

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Molecular and Cellular Probes

2014年28卷4期

118-122页

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High creatine kinase levels and white matter changes: Clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiency

Molecular and Cellular Probes

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High creatine kinase levels and white matter changes: Clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiency

Molecular and Cellular Probes

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Molecular and Cellular Probes

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