Analysis of the RPGRGene in 11 Pedigrees with the Retinitis Pigmentosa Type 3 Genotype: Paucity of Mutations in the Coding Region but Splice Defects in Two Families
Open Access
- 1 September 1997
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 61 (3) , 571-580
- https://doi.org/10.1086/515523
Abstract
No abstract availableKeywords
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