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Wiley Open Access, Molecular Genetics and Genomic Medicine, 7(8), 2020

DOI: 10.1002/mgg3.1229

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The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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