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زیست شناسی::
افتالموپلژی پیشرونده خارجی
syndrome (KSS), Pearson Syndrome, or progressive external ophthalmoplegia
(PEO).
On the other hand, multiple deletions of mtDNA have been reported in familial forms of progressive external ophthalmoplegia (PEO) with both autosomal dominant and recessive inheritance.
RRM2B, OPA1, and MFN2 genes have been associated with PEO syndrome and
The genetic background of autosomal recessive progressive external ophthalmoplegia (PEO) is mostly unknown, with POLG being the only associated gene
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