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Phenotype of autosomal dominant retinitis pigmentosa associated with the S50T mutation in the NRL gene.
Phenotype of autosomal dominant retinitis pigmentosa associated with the S50T mutation in the NRL gene.
2000
Dar Bessant
Annette M Payne
Ge Holder
F. W. Fitzke
Ss Bhattachayra
A. C. Bird
Keywords:
Autosomal dominant retinitis pigmentosa
Gene
Genetics
Phenotype
Biology
Mutation
Correction
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