4.2 Meeting Abstract

Rare inherited mitochondrial neuropathies with recessive mutations in MPV17 and SCO2 identified by whole exome sequencing

Journal

JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
Volume 26, Issue 1, Pages 130-131

Publisher

WILEY

Keywords

Mitochondrial neuropathy; MPV17; SCO2; Non-syndromic HMSN; Whole exome sequencing

Ask authors/readers for more resources

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available