A distinct mitochondrial myopathy, lactic acidosis and sideroblastic anemia (MLASA) phenotype associates with YARS2 mutations

✍ Scribed by Shahni, Rojeen; Wedatilake, Yehani; Cleary, Maureen A.; Lindley, Keith J.; Sibson, Keith R.; Rahman, Shamima

• Book ID: 121228209
• Publisher: John Wiley and Sons
• Year: 2013
• Tongue: English
• Weight: 247 KB
• Volume: 161
• Category: Article
• ISSN: 1552-4825
• DOI: 10.1002/ajmg.a.36065