Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2020 Nov 24;89(2):280–292. doi: 10.1002/ana.25951

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© 2020 The Authors. Annals of Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.

This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

PMC Copyright notice

Genomic distribution of the analyzed mutations based on the quantity of dystrophin expressed. (A) Canonical splice site mutations. (B) Pseudoexon and noncanonical splice site mutations. (C) Nonsense mutations within “in‐frame” exons. DMD exons and introns 1 to 79 are symbolized by spheres and connecting lines from black to gray in repeats of 10. Mutations of the patients of group A, group B, and group C appear on the top of the respective exons/introns. Each sphere represents 1 patient.