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Association of mitochondrial copy number variation and T16189C polymorphism with colorectal cancer i...

Association of mitochondrial copy number variation and T16189C polymorphism with colorectal cancer i...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_b56dc0d762d846c088b2a2b21e82d0d9

Association of mitochondrial copy number variation and T16189C polymorphism with colorectal cancer in North Indian population

About this item

Full title

Association of mitochondrial copy number variation and T16189C polymorphism with colorectal cancer in North Indian population

Publisher

London, England: SAGE Publications

Journal title

Tumor biology, 2017-11, Vol.39 (11), p.101042831774029-1010428317740296

Language

English

Formats

Publication information

Publisher

London, England: SAGE Publications

More information

Scope and Contents

Contents

Globally, colorectal cancer is the third most common type of cancer. Genetic instability leading to cancer development is one of the major causes for development of cancer. Alterations in mitochondrial genome, that is, mutations, single-nucleotide polymorphisms, and copy number variations are known to contribute in cancer development. The aim of ou...

Alternative Titles

Full title

Association of mitochondrial copy number variation and T16189C polymorphism with colorectal cancer in North Indian population

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_b56dc0d762d846c088b2a2b21e82d0d9

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_b56dc0d762d846c088b2a2b21e82d0d9

Other Identifiers

ISSN

1010-4283

E-ISSN

1423-0380

DOI

10.1177/1010428317740296

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