Rhodopsin mutation proline³⁴⁷-to-alanine in a family with autosomal dominant retinitis pigmentosa indicates an important role for proline at position 347

Abstract

Journal Article Rhodopsin mutation proline347-to-alanine in a family with autosomal dominant retinitis pigmentosa indicates an important role for proline at position 347 Get access Jennifer P. Macke, Jennifer P. Macke 1Department of Molecular Biology and Genetics, Howard Hughes Medical Institute, Johns Hopkins University School of Medicine725 North Wolle Street, MD 21205, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar Jill C. Hennessey, Jill C. Hennessey 2National Retinitis Pigmentosa Foundation, BaltimoreMD 21205, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar Jeremy Nathans Jeremy Nathans * 1Department of Molecular Biology and Genetics, Howard Hughes Medical Institute, Johns Hopkins University School of Medicine725 North Wolle Street, MD 21205, USA3Department of Neuroscience and Department of Ophthalmology, Howard Hughes Medical Institute, Johns Hopkins University School of Medicine725 North Wolle Street, MD 21205, USA *To whom correspondence should be addressed Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 4, Issue 4, April 1995, Pages 775–776, https://doi.org/10.1093/hmg/4.4.775 Published: 01 April 1995 Article history Received: 04 January 1995 Revision received: 31 January 1995 Accepted: 31 January 1995 Published: 01 April 1995