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Orphanet Journal of Rare Diseases
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November 14, 2020
Compound heterozygous inheritance of two novel COQ2 variants results in familial coenzyme Q deficiency
Aliaa H Abdelhakim, Avinash V Dharmadhikari, Sara D Ragi, et al.
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of 2
Search research articles
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Showing results (11-20 of 11) with videos related to
Sort By:
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Orphanet Journal of Rare Diseases
|
November 14, 2020
Compound heterozygous inheritance of two novel COQ2 variants results in familial coenzyme Q deficiency
Aliaa H Abdelhakim, Avinash V Dharmadhikari, Sara D Ragi, et al.
Page
of 2