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Molecular Genetics & Genomic Medicine
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May 1, 2020
The KLHL40 c.1516A>C is a Chinese-specific founder mutation causing nemaline myopathy 8: Report of six patients with pre- and postnatal phenotypes
Kit San Yeung, Florrie N Y Yu, Cheuk Wing Fung, et al.
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Showing results (21-30 of 21) with videos related to
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Molecular Genetics & Genomic Medicine
|
May 1, 2020
The KLHL40 c.1516A>C is a Chinese-specific founder mutation causing nemaline myopathy 8: Report of six patients with pre- and postnatal phenotypes
Kit San Yeung, Florrie N Y Yu, Cheuk Wing Fung, et al.
Page
of 3