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DMD‐related muscular dystrophy in Cameroon: Clinical and genetic profiles

DMD‐related muscular dystrophy in Cameroon: Clinical and genetic profiles

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_a188fa4720c845e5b4be51673534db5a

DMD‐related muscular dystrophy in Cameroon: Clinical and genetic profiles

About this item

Full title

DMD‐related muscular dystrophy in Cameroon: Clinical and genetic profiles

Publisher

United States: John Wiley & Sons, Inc

Journal title

Molecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1362-n/a

Language

English

Formats

Publication information

Publisher

United States: John Wiley & Sons, Inc

More information

Scope and Contents

Contents

Background
Most of the previous studies on Duchenne Muscular Dystrophy (DMD) were conducted in Caucasian, Asian, and Arab populations. Therefore, little is known about the features of this disease in Africans. In this study, we aimed to determine the clinical characteristics of DMD, and the common mutations associated with this condition in a gr...

Alternative Titles

Full title

DMD‐related muscular dystrophy in Cameroon: Clinical and genetic profiles

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_a188fa4720c845e5b4be51673534db5a

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_a188fa4720c845e5b4be51673534db5a

Other Identifiers

ISSN

2324-9269

E-ISSN

2324-9269

DOI

10.1002/mgg3.1362

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