Novel mutations seen in rapid, fatal case of early onset LAL deficiency (Wolman disease)

✍ Scribed by Gomez-Najera, Mariana; Barajas-Medina, Hilario; Gallegos-Rivas, Mayra Celina; Mendez-Sashida, Pedro; Simonds, Amy; Tripuraneni, Radhika; Valles-Ayoub, Yadira; Eroglu, Yasemen

• Book ID: 122743556
• Publisher: Elsevier Science
• Year: 2013
• Tongue: English
• Weight: 130 KB
• Volume: 108
• Category: Article
• ISSN: 1096-7192
• DOI: 10.1016/j.ymgme.2012.11.100