Exclusion of two candidate loci for autosomal recessive nemaline myopathy.

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...

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Hlavní autoři: Tahvanainen, E, Beggs, A H, Wallgren-Pettersson, C
Médium: Artigo
Jazyk:Inglês
Vydáno: 1994
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1049608/
https://ncbi.nlm.nih.gov/pubmed/8151647
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