Paramyotonia congenita and myotonic dystrophy are not allelic disorders.

M Koch,H Harley,T Grimm,M Sarfarazi,B Müller,B Zoll,P S Harper

CYTOGENETICS AND CELL GENETICS（1989）

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摘要

More recently it was shown that DM is closely linked to the apolipoprotein C2 gene. These data place the mutation for DM within 5 cM of the APOC2 gene. To verify the clinical suggestion and the results of the membrane studies that DM and PC are genetically distinct disorders, we carried out a linkage study with the APOC2 gene probe

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