Identification of Biallelic dystrophin gene variants during maternal carrier testing for Becker muscular dystrophy and review of the <i>DMD</i> exon 49–51 deletion phenotype-Reference-Cited by-同舟云学术

Identification of Biallelic dystrophin gene variants during maternal carrier testing for Becker muscular dystrophy and review of the DMD exon 49–51 deletion phenotype

Published:2022-11-24 Issue:1 Volume:11 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Ulm Elizabeth A.¹^ORCID,Nagaraj Chinmayee B.¹²,Tian Cuixia²³,Smolarek Teresa A.¹³

Affiliation:

1. Division of Human Genetics Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA

2. Division of Neurology Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA

3. Department of Pediatrics University of Cincinnati School of Medicine Cincinnati Ohio USA

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.2088

Reference34 articles.

1. A Genotype-Phenotype Correlation Study of Exon Skip-Equivalent In-Frame Deletions and Exon Skip-Amenable Out-of-Frame Deletions across the DMD Gene to Simulate the Effects of Exon-Skipping Therapies: A Meta-Analysis

2. Cognitive and Neurobehavioral Profile in Boys With Duchenne Muscular Dystrophy

3. Deletion mutations in DMD gene and disease phenotype among Saudi patients with Duchenne muscular dystrophy;Chaudhary A. G.;Middle‐East Journal of Scientific Research,2009

4. The CINRG Becker Natural History Study: Baseline characteristics

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