Molecular and Pathological Analyses of IARS1-Deficient Mice: An IARS Disorder Model
Molecular and Pathological Analyses of IARS1-Deficient Mice: An IARS Disorder Model
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Publisher
Switzerland: MDPI AG
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Language
English
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Publisher
Switzerland: MDPI AG
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Contents
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 mutations in the IARS1 gene. Although severe prenatal-onset growth retardation and...
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Full title
Molecular and Pathological Analyses of IARS1-Deficient Mice: An IARS Disorder Model
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10138339
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10138339
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ISSN
1422-0067
E-ISSN
1422-0067
DOI
10.3390/ijms24086955
