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  • A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population

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A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population

Authors

  1. Correspondence to:
 Dr F P M Cremers Department of Human Genetics, University Medical Centre Nijmegen, PO Box 9101, 6500 HB Nijmegen, Netherlands;
 f.cremers{at}antrg.umcn.nl
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Citation

Yzer S, van den Born LI, Schuil J, et al
A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population
Journal of Medical Genetics 2003;40:709-713.

Publication history

  • First published September 5, 2003.
Online issue publication 
April 27, 2016

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Copyright 2003 Journal of Medical Genetics