Clinical and molecular analysis of four unrelated Chinese families with pathogenic KLHL40 variants causing nemaline myopathy 8

Overview of attention for article published in Orphanet Journal of Rare Diseases, April 2022

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Clinical and molecular analysis of four unrelated Chinese families with pathogenic KLHL40 variants causing nemaline myopathy 8 https://t.co/Muv3SqnMId https://t.co/XIvvMQAGs4

15 Apr 2022

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Clinical and molecular analysis of four unrelated Chinese families with pathogenic KLHL40 variants causing nemaline myopathy 8 https://t.co/b1AHI4X7ba

05 Apr 2022

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