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Annals of Indian Academy of Neurology
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LETTER TO THE EDITOR
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A novel mutation in the clcn1 gene causing autosomal recessive myotonia congenita in siblings


 Department of Neurology, PGIMER, Chandigarh, India

Correspondence Address:
Sucharita Ray,
Department of Neurology, PGIMER, Chandigarh
India
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/aian.AIAN_970_20



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    -  Chakravarty K
    -  Lal V
    -  Ray S
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