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Anoctamin 5 (ANO5) Muscle Disorders: A Narrative Review

Anoctamin 5 (ANO5) Muscle Disorders: A Narrative Review

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9602132

Anoctamin 5 (ANO5) Muscle Disorders: A Narrative Review

About this item

Full title

Anoctamin 5 (ANO5) Muscle Disorders: A Narrative Review

Publisher

Switzerland: MDPI AG

Journal title

Genes, 2022-09, Vol.13 (10), p.1736

Language

English

Formats

Publication information

Publisher

Switzerland: MDPI AG

More information

Scope and Contents

Contents

Anoctaminopathy-5 refers to a group of hereditary skeletal muscle or bone disorders due to mutations in the anoctamin 5 (ANO5)-encoding gene,
. ANO5 is a 913-amino acid protein of the anoctamin family that functions predominantly in phospholipid scrambling and plays a key role in the sarcolemmal repairing process. Monoallelic mutations in
giv...

Alternative Titles

Full title

Anoctamin 5 (ANO5) Muscle Disorders: A Narrative Review

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9602132

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9602132

Other Identifiers

ISSN

2073-4425

E-ISSN

2073-4425

DOI

10.3390/genes13101736

How to access this item