Molecular and Pathological Analyses of IARS1-Deficient Mice: An IARS Disorder Model
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DOI: 10.3390/ijms24086955
Abstract: Most mitochondrial diseases are hereditary and highly heterogeneous. Cattle born with the V79L mutation in the isoleucyl-tRNA synthetase 1 (IARS1) protein exhibit weak calf syndrome. Recent human genomic studies about pediatric mitochondrial diseases also identified… read more here.
Keywords: pathological analyses; molecular pathological; mutant mice; analyses iars1 ... See more keywords