Matches in Nanopublications for { ?s ?p "[Mutation screening of AGK in further individuals with congenital cataracts and cardiomyopathy identified numerous loss-of-function mutations in an additional eight families, confirming the causal nature of AGK deficiency in Sengers syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP213370.RAzyQi5hfBmkT1K6eUbR5Q_phMAw5dbCwarIlvlEgarQc130_assertion description "[Mutation screening of AGK in further individuals with congenital cataracts and cardiomyopathy identified numerous loss-of-function mutations in an additional eight families, confirming the causal nature of AGK deficiency in Sengers syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213370.RAzyQi5hfBmkT1K6eUbR5Q_phMAw5dbCwarIlvlEgarQc130_provenance.
- NP808860.RAWVywmZxWNBzy7z63p_o55pLGiM1aV3xWeQXs3nzt9Q8130_assertion description "[Mutation screening of AGK in further individuals with congenital cataracts and cardiomyopathy identified numerous loss-of-function mutations in an additional eight families, confirming the causal nature of AGK deficiency in Sengers syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP808860.RAWVywmZxWNBzy7z63p_o55pLGiM1aV3xWeQXs3nzt9Q8130_provenance.
- NP870298.RAQ-oX9zJOLi7Zi_LDfXMozJJVI8pWNJsqGA_5XEuyqAs130_assertion description "[Mutation screening of AGK in further individuals with congenital cataracts and cardiomyopathy identified numerous loss-of-function mutations in an additional eight families, confirming the causal nature of AGK deficiency in Sengers syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870298.RAQ-oX9zJOLi7Zi_LDfXMozJJVI8pWNJsqGA_5XEuyqAs130_provenance.
- assertion description "[Mutation screening of AGK in further individuals with congenital cataracts and cardiomyopathy identified numerous loss-of-function mutations in an additional eight families, confirming the causal nature of AGK deficiency in Sengers syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutation screening of AGK in further individuals with congenital cataracts and cardiomyopathy identified numerous loss-of-function mutations in an additional eight families, confirming the causal nature of AGK deficiency in Sengers syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP956567.RAcLh4TCWclPaGOpR4VkvwlztGqdwx-NGebD0pw2uWjuw130_assertion description "[Mutation screening of AGK in further individuals with congenital cataracts and cardiomyopathy identified numerous loss-of-function mutations in an additional eight families, confirming the causal nature of AGK deficiency in Sengers syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP956567.RAcLh4TCWclPaGOpR4VkvwlztGqdwx-NGebD0pw2uWjuw130_provenance.
- NP920809.RAq1zgVrmX0Di4N3r20I49TPcielQCvWAiPoLFNl6SJRs130_assertion description "[Mutation screening of AGK in further individuals with congenital cataracts and cardiomyopathy identified numerous loss-of-function mutations in an additional eight families, confirming the causal nature of AGK deficiency in Sengers syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920809.RAq1zgVrmX0Di4N3r20I49TPcielQCvWAiPoLFNl6SJRs130_provenance.
- NP920821.RArYYp9j3sM4Zm214b8BQs-nD8Zpu2U-h5MwhujSU2vb8130_assertion description "[Mutation screening of AGK in further individuals with congenital cataracts and cardiomyopathy identified numerous loss-of-function mutations in an additional eight families, confirming the causal nature of AGK deficiency in Sengers syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920821.RArYYp9j3sM4Zm214b8BQs-nD8Zpu2U-h5MwhujSU2vb8130_provenance.
- NP956569.RAiilhG9hP6hUBLH3d6LZMF18QhKJnHospDJag5KClbCQ130_assertion description "[Mutation screening of AGK in further individuals with congenital cataracts and cardiomyopathy identified numerous loss-of-function mutations in an additional eight families, confirming the causal nature of AGK deficiency in Sengers syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP956569.RAiilhG9hP6hUBLH3d6LZMF18QhKJnHospDJag5KClbCQ130_provenance.