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Published in 2019 at "Annals of Clinical and Translational Neurology"
DOI: 10.1002/acn3.50910
Abstract: CAPN3 mutations cause a limb girdle muscular dystrophy. Functional characterization of novel mutations facilitates diagnosis of future cases. We have identified a novel (c.1992 + 2T>G) CAPN3 mutation that disrupts the donor splice site of…
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Keywords:
capn3 roma;
novel intronic;
capn3;
intronic capn3 ... See more keywords