Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in the southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A

✍ Scribed by Zhi-Qiang Wang; Xue-Jiao Chen; Shen-Xing Murong; Ning Wang; Zhi-Ying Wu

• Book ID: 116779223
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 115 KB
• Volume: 71
• Category: Article
• ISSN: 0168-0102
• DOI: 10.1016/j.neures.2011.07.844