Matches in Nanopublications for { ?s ?p "[The purpose of this study was to determine the frequency and spectrum of inosine monophosphate dehydrogenase type I (IMPDH1) mutations associated with autosomal dominant retinitis pigmentosa (RP), to determine whether mutations in IMPDH1 cause other forms of inherited retinal degeneration, and to analyze IMPDH1 mutations for alterations in enzyme activity and nucleic acid binding.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP734363.RAC83EfKY3jP6NPIuW79UiHyvXeU89Ul-2thVEaXcuQ6o130_assertion description "[The purpose of this study was to determine the frequency and spectrum of inosine monophosphate dehydrogenase type I (IMPDH1) mutations associated with autosomal dominant retinitis pigmentosa (RP), to determine whether mutations in IMPDH1 cause other forms of inherited retinal degeneration, and to analyze IMPDH1 mutations for alterations in enzyme activity and nucleic acid binding.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734363.RAC83EfKY3jP6NPIuW79UiHyvXeU89Ul-2thVEaXcuQ6o130_provenance.
- NP592130.RAfoFeLQcVQZtjuMOnZ-v9r9PppfheyeZ_sNRTHanwwW4130_assertion description "[The purpose of this study was to determine the frequency and spectrum of inosine monophosphate dehydrogenase type I (IMPDH1) mutations associated with autosomal dominant retinitis pigmentosa (RP), to determine whether mutations in IMPDH1 cause other forms of inherited retinal degeneration, and to analyze IMPDH1 mutations for alterations in enzyme activity and nucleic acid binding.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592130.RAfoFeLQcVQZtjuMOnZ-v9r9PppfheyeZ_sNRTHanwwW4130_provenance.