Matches in Nanopublications for { ?s ?p "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP450990.RACaQAFJLWQXS-VBQ5NjkZZKFb_7kZ-t2uPT_OZi169ho130_assertion description "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450990.RACaQAFJLWQXS-VBQ5NjkZZKFb_7kZ-t2uPT_OZi169ho130_provenance.
- NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_assertion description "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_provenance.
- assertion description "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1009179.RAdUiRNICNsHHLE3fICkyb79ki-qHD0POEdZLBBOU9OBU130_assertion description "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1009179.RAdUiRNICNsHHLE3fICkyb79ki-qHD0POEdZLBBOU9OBU130_provenance.
- NP1009190.RAR50m2GO7_8XHSj-Q6VPLvRmNr-YSziaNQhErRQg6eto130_assertion description "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1009190.RAR50m2GO7_8XHSj-Q6VPLvRmNr-YSziaNQhErRQg6eto130_provenance.
- NP528884.RACpUIJP0gojjfr-BBT44dt9jNlvh-fyYmEARS2qGPKBA130_assertion description "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528884.RACpUIJP0gojjfr-BBT44dt9jNlvh-fyYmEARS2qGPKBA130_provenance.
- NP528883.RAWEyL3yM-O16bq5MiYPAA0NhOww61VVk3KbD1xyiCs4I130_assertion description "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528883.RAWEyL3yM-O16bq5MiYPAA0NhOww61VVk3KbD1xyiCs4I130_provenance.
- NP528889.RAZrHQYSWcNJXsnZJ_k_MRWhKuFHYkYE-GN7FFGB6q3EA130_assertion description "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528889.RAZrHQYSWcNJXsnZJ_k_MRWhKuFHYkYE-GN7FFGB6q3EA130_provenance.
- NP528890.RAs2XPuUAko3tTxVZCtZrKoHWOg6-JK3jcTcZgF4ycye4130_assertion description "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528890.RAs2XPuUAko3tTxVZCtZrKoHWOg6-JK3jcTcZgF4ycye4130_provenance.
- NP509538.RAJiju141g_2k7dSqw8PMePqzN19D9grX0BEBZ1nL5yfg130_assertion description "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP509538.RAJiju141g_2k7dSqw8PMePqzN19D9grX0BEBZ1nL5yfg130_provenance.
- NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_assertion description "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_provenance.