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Christof Meyer-Kleine

University of Marburg

5

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308

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Spectrum of mutations in the major human skeletal muscle chloride channel gene (CLCN1) leading to myotonia

1995 American Journal of Human Genetics
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SpectrumofMutations intheMajorHuman Skeletal Muscle Chloride ChannelGene(CLCNI)Leading toMyotonia

1995
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Genomic organization of the human muscle chloride channel CIC-1 and analysis of novel mutations leading to Becker-type myotonia

1994 Human Molecular Genetics
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Molecular and genetic characterisation of German families with paramyotonia congenita and demonstration of founder effect in the Ravensberg families

1994 Human Genetics
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A recurrent 14 bp deletion in the CLCN1 gene associated with generalized myotonia (Becker)

1994 Human Molecular Genetics
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