A single mutation in MCCC1 or MCCC2 as a potential cause of positive screening for 3-methylcrotonyl-CoA carboxylase deficiency

Authors

Keywords

Journal

Volume 105, Issue 4, Pages 602-606

Publisher

Elsevier BV

Online

2012-01-01

DOI

10.1016/j.ymgme.2011.12.018

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

Upload Now

The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.

Get Started