Retinal Dystrophy Due to Paternal Isodisomy for Chromosome 1 or Chromosome 2, with Homoallelism for Mutations in RPE65 or MERTK, Respectively

✍ Scribed by Debra A. Thompson; Christina L. McHenry; Yun Li; Julia E. Richards; Mohammad I. Othman; Eberhard Schwinger; Douglas Vollrath; Samuel G. Jacobson; Andreas Gal

• Book ID: 119770015
• Publisher: American Society of Human Genetics
• Year: 2002
• Tongue: English
• Weight: 90 KB
• Volume: 70
• Category: Article
• ISSN: 0002-9297
• DOI: 10.1086/338455