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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

Author:

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

Publication:

The American Journal of Human Genetics

Publisher:

Elsevier

Date:

January 2002

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