Type III 3-Methylglutaconic Aciduria (Optic Atrophy Plus Syndrome, or Costeff Optic Atrophy Syndrome): Identification of the OPA3 Gene and Its Founder Mutation in Iraqi Jews

✍ Scribed by Yair Anikster; Robert Kleta; Avraham Shaag; William A. Gahl; Orly Elpeleg

• Book ID: 117853765
• Publisher: American Society of Human Genetics
• Year: 2001
• Tongue: English
• Weight: 123 KB
• Volume: 69
• Category: Article
• ISSN: 0002-9297
• DOI: 10.1086/324651