Homozygous V377I mutation causing mevalonate kinase | BMJ Case Reports

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Case Reports: Rare disease

Homozygous V377I mutation causing mevalonate kinase

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Cite this article as:: Brito T, Banganho D, Pedrosa C, et al

Homozygous V377I mutation causing mevalonate kinase

BMJ Case Reports CP 2022;15:e249135.