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. 1991 Dec 25;19(24):6982. doi: 10.1093/nar/19.24.6982-a

A sequence polymorphism in the human peripherin/RDS gene

GJ Farrar ¹, P Kenna ¹, SA Jordan ¹, R Kumar-Singh ¹, P Humphries ¹

PMCID: PMC329383 PMID: 1762948

Abstract

6982

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Farrar G. J., Kenna P., Redmond R., McWilliam P., Bradley D. G., Humphries M. M., Sharp E. M., Inglehearn C. F., Bashir R., Jay M. Autosomal dominant retinitis pigmentosa: absence of the rhodopsin proline----histidine substitution (codon 23) in pedigrees from Europe. Am J Hum Genet. 1990 Dec;47(6):941–945. [PMC free article] [PubMed] [Google Scholar]
Travis G. H., Christerson L., Danielson P. E., Klisak I., Sparkes R. S., Hahn L. B., Dryja T. P., Sutcliffe J. G. The human retinal degeneration slow (RDS) gene: chromosome assignment and structure of the mRNA. Genomics. 1991 Jul;10(3):733–739. doi: 10.1016/0888-7543(91)90457-p. [DOI] [PubMed] [Google Scholar]

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