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Retinal Dystrophy Due to Paternal Isodisomy for Chromosome 1 or Chromosome 2, with Homoallelism for Mutations in RPE65 or MERTK, Respectively
Debra A. Thompson, Christina L. McHenry, Yun Li, Julia E. Richards, Mohammad I. Othman, Eberhard Schwinger, Douglas Vollrath, Samuel G. Jacobson, Andreas GalVolume:
70
Year:
2002
Language:
english
DOI:
10.1086/338455
File:
PDF, 90 KB
english, 2002