Interplay between DMD Point Mutations and Splicing Signals in Dystrophinopathy Phenotypes-Reference-Cited by-同舟云学术

Interplay between DMD Point Mutations and Splicing Signals in Dystrophinopathy Phenotypes

Published:2013-03-25 Issue:3 Volume:8 Page:e59916
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Juan-Mateu Jonàs,González-Quereda Lidia,Rodríguez Maria José,Verdura Edgard,Lázaro Kira,Jou Cristina,Nascimento Andrés,Jiménez-Mallebrera Cecilia,Colomer Jaume,Monges Soledad,Lubieniecki Fabiana,Foncuberta Maria Eugenia,Pascual-Pascual Samuel Ignacio,Molano Jesús,Baiget Montserrat,Gallano Pia

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

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4. Exploring the molecular basis for variability among patients with becker muscular dystrophy: Dystrophin gene and protein studies;AH Beggs;American Journal of Human Genetics,1991

5. An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus;AP Monaco;Genomics,1988

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