A novel homozygous RRM2B missense mutation in association with severe mtDNA depletion

Published 2009 View Full Article

  1. Home
  2. Publications
  3. Publication Search
  4. Publication Details
Title
A novel homozygous RRM2B missense mutation in association with severe mtDNA depletion
Authors
Keywords
-
Journal
NEUROMUSCULAR DISORDERS
Volume 19, Issue 2, Pages 147-150
Publisher
Elsevier BV
Online
2009-01-13
DOI
10.1016/j.nmd.2008.11.014

Ask authors/readers for more resources

Protocol

Community support

Reagent

Community support

Reprint

Contact the author

Add your recorded webinar

Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.

Upload Now

Ask a Question. Answer a Question.

Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.

Get Started
Webinars Posters Questions Hubs Funding Journals Articles Connect Collections Reviewers About Us FAQs Mobile App Privacy Policy Terms of Use
© Peeref 2019-2024. All rights reserved.