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Cellular Models for Primary CoQ Deficiency Pathogenesis Study

Cellular Models for Primary CoQ Deficiency Pathogenesis Study

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8508219

Cellular Models for Primary CoQ Deficiency Pathogenesis Study

About this item

Full title

Cellular Models for Primary CoQ Deficiency Pathogenesis Study

Publisher

Basel: MDPI AG

Journal title

International journal of molecular sciences, 2021-10, Vol.22 (19), p.10211

Language

English

Formats

Publication information

Publisher

Basel: MDPI AG

More information

Scope and Contents

Contents

Primary coenzyme Q10 (CoQ) deficiency includes a heterogeneous group of mitochondrial diseases characterized by low mitochondrial levels of CoQ due to decreased endogenous biosynthesis rate. These diseases respond to CoQ treatment mainly at the early stages of the disease. The advances in the next generation sequencing (NGS) as whole-exome sequenci...

Alternative Titles

Full title

Cellular Models for Primary CoQ Deficiency Pathogenesis Study

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8508219

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8508219

Other Identifiers

ISSN

1422-0067,1661-6596

E-ISSN

1422-0067

DOI

10.3390/ijms221910211

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