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Logo of jmedgeneJournal of Medical GeneticsCurrent TOCInstructions for authors
 
J Med Genet. Jan 1994; 31(1): 79–80.
PMCID: PMC1049608
Exclusion of two candidate loci for autosomal recessive nemaline myopathy.
E Tahvanainen, A H Beggs, and C Wallgren-Pettersson
Department of Medical Genetics, University of Helsinki, Finland.
Abstract
The putative gene for autosomal recessive nemaline myopathy has not been mapped, cloned, or otherwise characterised. We used linkage analysis with polymorphic CA repeats to test for the involvement of two candidate loci, APOA2 and ACTN2. Based on the segregation in five families both candidate loci could be excluded.
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