(2018). Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1. Mol Genet Genomic Med.
Chicago Style aipamena"Whole Exome Sequencing of a Patient With Suspected Mitochondrial Myopathy Reveals Novel Compound Heterozygous Variants in RYR1." Mol Genet Genomic Med 2018.
MLA aipamena"Whole Exome Sequencing of a Patient With Suspected Mitochondrial Myopathy Reveals Novel Compound Heterozygous Variants in RYR1." Mol Genet Genomic Med 2018.
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