Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood

Title
Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 83, Issue 4, Pages 489-494
Publisher
Elsevier BV
Online
2008-09-26
DOI
10.1016/j.ajhg.2008.09.002

Ask authors/readers for more resources

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