The Lack of the Celf2a Splicing Factor Converts a Duchenne Genotype Into a Becker Phenotype

Nature Communications - United Kingdom
doi 10.1038/ncomms10488
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

Heterozygous Glucokinase Splicing Mutation - Identical Genotype With Variable Phenotype in a Single Family

Endocrine Abstracts
2015English

Improved Diagnosis of Duchenne/Becker Muscular Dystrophy.

Journal of Clinical Investigation
Medicine
1990English

Expanding the Phenotype Half of the Genotype−phenotype Space

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2016English

Prevalence of Duchenne and Becker Muscular Dystrophies in the United States

Pediatrics
Child HealthPediatricsPerinatology
2015English

Expanding the Phenotype of DST‐related Disorder: A Case Report Suggesting a Genotype/Phenotype Correlation

American Journal of Medical Genetics, Part A
Genetics
2019English

Genotype-Phenotype Relationships in a Cohort

European Respiratory Journal
MedicinePulmonaryRespiratory Medicine
1996English

Motor Clinical Progression in a Series of Pediatric Duchenne and Becker Muscular Dystrophy Cases

Paediatrica Indonesiana
2019English

The Enumeration of Genotype-Phenotype Correspondences

Heredity
Genetics
1957English

213 Initial Explorations Into Genotype-Phenotype Correlations in Psoriasis: The Homozygous Recessive Model

Journal of Investigative Dermatology
BiochemistryDermatologyCell BiologyMolecular Biology
2017English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy