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  • curprev 22:34, 21 November 2024‎ Houstonmendoza6491 talk contribs‎ 7,198 bytes +7,198‎ Created page with "BACKGROUND Autosomal recessive or compound heterozygous mutations in KLHL40 cause nemaline myopathy 8, which is one of the most severe forms of nemaline myopathy. The KLHL40 c..."
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