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POLG-related disorders and their neurological manifestations

POLG-related disorders and their neurological manifestations

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8796686

POLG-related disorders and their neurological manifestations

About this item

Full title

POLG-related disorders and their neurological manifestations

Publisher

London: Nature Publishing Group UK

Journal title

Nature reviews. Neurology, 2019-01, Vol.15 (1), p.40-52

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

The
POLG
gene encodes the mitochondrial DNA polymerase that is responsible for replication of the mitochondrial genome. Mutations in
POLG
can cause early childhood mitochondrial DNA (mtDNA) depletion syndromes or later-onset syndromes arising from mtDNA deletions.
POLG
mutations are the most common cause of inherited mitochondrial...

Alternative Titles

Full title

POLG-related disorders and their neurological manifestations

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8796686

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8796686

Other Identifiers

ISSN

1759-4758,1759-4766

E-ISSN

1759-4766

DOI

10.1038/s41582-018-0101-0

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