GP126 Large Deletions inDMDgene Is the Most Prevalence Mutation in Russian Children With Duchenne Muscular Dystrophy

doi 10.1136/archdischild-2019-epa.191
Full Text
Abstract

Available in full text

Date
Authors
Publisher

BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health

Related search

Is Molecular Diagnosis Necessary for Children With Duchenne Muscular Dystrophy?

Indian Pediatrics
Child HealthPediatricsPerinatology
2019English

Bone Health in Children With Duchenne Muscular Dystrophy: A Review

Pediatrics & Therapeutics
2015English

Duchenne Muscular Dystrophy

Physiotherapy
Physical TherapySports TherapyRehabilitation
1990English

On the Origin of Deletions and Point Mutations in Duchenne Muscular Dystrophy: Most Deletions Arise in Oogenesis and Most Point Mutations Result From Events in Spermatogenesis.

Journal of Medical Genetics
Genetics
1994English

Duchenne Muscular Dystrophy

English

Duchenne Muscular Dystrophy

Methods in Molecular Biology
GeneticsMolecular Biology
2018English

Duchenne Muscular Dystrophy

2020English

Echinocytes in Families With Duchenne Muscular Dystrophy.

Journal of Medical Genetics
Genetics
1977English

Incidence of Duchenne Muscular Dystrophy Is Associated With Social Deprivation

BMJ
2001English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy