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Open Access

Peer-reviewed

Research Article

Mutation spectrum analysis of Duchenne/Becker muscular dystrophy in 68 families in Kuwait: The era of personalized medicine

Fawziah Mohammed ,

Contributed equally to this work with: Fawziah Mohammed, Alaa Elshafey

Roles Conceptualization, Data curation, Formal analysis, Methodology, Writing – original draft

* E-mail: fawziahmam@hsc.edu.kw

Affiliation Medical Laboratory Sciences, Faculty of Allied Health Sciences, Kuwait University, Jabriah, Kuwait

http://orcid.org/0000-0003-3458-0288

⨯
Alaa Elshafey ,

Contributed equally to this work with: Fawziah Mohammed, Alaa Elshafey

Roles Conceptualization, Data curation, Formal analysis, Methodology, Writing – original draft

Affiliation Kuwait Medical Genetic Centre, Ministry of Health, Shouaikh, Kuwait
⨯
Haya Al-balool,

Roles Methodology

Affiliation Kuwait Medical Genetic Centre, Ministry of Health, Shouaikh, Kuwait
⨯
Hayat Alaboud,

Roles Methodology

Affiliation Kuwait Medical Genetic Centre, Ministry of Health, Shouaikh, Kuwait
⨯
Mohammed Al Ben Ali,

Roles Methodology

Affiliation Kuwait Medical Genetic Centre, Ministry of Health, Shouaikh, Kuwait
⨯
Adel Baqer,

Roles Methodology

Affiliation Kuwait Medical Genetic Centre, Ministry of Health, Shouaikh, Kuwait
⨯
Laila Bastaki

Roles Data curation, Supervision, Writing – review & editing

Affiliation Kuwait Medical Genetic Centre, Ministry of Health, Shouaikh, Kuwait
⨯

Mutation spectrum analysis of Duchenne/Becker muscular dystrophy in 68 families in Kuwait: The era of personalized medicine

Fawziah Mohammed,
Alaa Elshafey,
Haya Al-balool,
Hayat Alaboud,
Mohammed Al Ben Ali,
Adel Baqer,
Laila Bastaki

x

Published: May 30, 2018
https://doi.org/10.1371/journal.pone.0197205

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Dystrophin
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Point mutation
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Mutation databases
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Substitution mutation
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Deletion mutation
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Mutation
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Muscle proteins
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