Article info
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
- Dr Kaplan.
Citation
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
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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Copyright information
Journal of Medical Genetics