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Molecular and Pathological Analyses of IARS1-Deficient Mice: An IARS Disorder Model

Molecular and Pathological Analyses of IARS1-Deficient Mice: An IARS Disorder Model

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10138339

Molecular and Pathological Analyses of IARS1-Deficient Mice: An IARS Disorder Model

About this item

Full title

Molecular and Pathological Analyses of IARS1-Deficient Mice: An IARS Disorder Model

Publisher

Switzerland: MDPI AG

Journal title

International journal of molecular sciences, 2023-04, Vol.24 (8), p.6955

Language

English

Formats

Publication information

Publisher

Switzerland: MDPI AG

More information

Scope and Contents

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...

Alternative Titles

Full title

Molecular and Pathological Analyses of IARS1-Deficient Mice: An IARS Disorder Model

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10138339

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10138339

Other Identifiers

ISSN

1422-0067

E-ISSN

1422-0067

DOI

10.3390/ijms24086955

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