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  • Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evidence of clinical heterogeneity at this locus

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Original article
Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evidence of clinical heterogeneity at this locus
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Authors

  1. Dr Kaplan.
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Citation

Rozet J, Gerber S, Ghazi I, et al
Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evidence of clinical heterogeneity at this locus
Journal of Medical Genetics 1999;36:447-451.

Publication history

  • Received November 23, 1998
  • Revised March 1, 1999
  • First published June 1, 1999.
Online issue publication 
June 01, 1999

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Journal of Medical Genetics