P123 Rare hereditary cardiomyopathy caused by novel homozygous mutation in the myl3 gene | Archives of Disease in Childhood

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P123 Rare hereditary cardiomyopathy caused by novel homozygous mutation in the myl3 gene

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Cite this article as:: V L, N V, N Z, et al

P123 Rare hereditary cardiomyopathy caused by novel homozygous mutation in the myl3 gene

Archives of Disease in Childhood 2017;102:A81-A82.