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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| Description | scientific article |
| Author/s |
author: Arnold Munnich |
| Publication date | June 1, 1999 |
| Language | English |
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