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Dive into the research topics of 'Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy'. Together they form a unique fingerprint.- Sort by
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Senda Ajroud-Driss*, Faisal Fecto, Kaouther Ajroud, Irfan Lalani, Sarah E. Calvo, Vamsi K. Mootha, Han Xiang Deng, Nailah Siddique, Albert J. Tahmoush, Terry D. Heiman-Patterson, Teepu Siddique
Research output: Contribution to journal › Article › peer-review