P.17.11 c.250G>A in ETFDH, a common sequence variant in southern Chinese population is a pathogenic mutation to cause multiple acyl-CoA dehydrogenase deficiency

✍ Scribed by Liang, W.C.; Lin, Y.F.; Liu, D.Y.; Nishino, I.; Jong, Y.J.

• Book ID: 121901222
• Publisher: Elsevier Science
• Year: 2013
• Tongue: English
• Weight: 50 KB
• Volume: 23
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2013.06.661