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High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany
Based on previous reports the frequency of co-segregating recessive chloride channel (CLCN1) mutations in families with myotonic dystrophy type 2 (DM2) was suspected to be increased. We have studied the frequency of CLCN1 mutations in two separate patient and control cohorts from Germany and Finland...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4079033/ https://ncbi.nlm.nih.gov/pubmed/18807109 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00415-008-0010-z |
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