Mutational spectrum and phenotypic variability of Duchenne muscular dystrophy and related disorders in a Bangladeshi population

Mutational spectrum and phenotypic variability of Duchenne muscular dystrophy and related disorders in a Bangladeshi population

Abstract Duchenne muscular dystrophy (DMD) is a severe rare neuromuscular disorder caused by mutations in the X-linked dystrophin gene. Several mutations have been identified, yet the full mutational spectrum, and their phenotypic consequences, will require genotyping across different populations. T...

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Prif Awduron: Shaoli Sarker, Tamannyat Binte Eshaque, Anjana Soorajkumar, Nasna Nassir, Binte Zehra, Shayla Imam Kanta, Md Atikur Rahaman, Amirul Islam, Shimu Akter, Mohammad Kawsar Ali, Rabeya Akter Mim, K. M. Furkan Uddin, Mohammod Shah Jahan Chowdhury, Nusrat Shams, Md. Abdul Baqui, Elaine T. Lim, Hosneara Akter, Marc Woodbury-Smith, Mohammed Uddin
Fformat: Erthygl
Iaith:English
Cyhoeddwyd: Nature Portfolio 2023-12-01
Cyfres:Scientific Reports
Mynediad Ar-lein:https://doi.org/10.1038/s41598-023-48982-w

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https://doi.org/10.1038/s41598-023-48982-w

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