Matches in Nanopublications for { ?s ?p "[Exon deletion in the non-catalytic domain of eIF2Bepsilon due to a splice site mutation leads to infantile forms of CACH/VWM with severe decrease of eIF2B GEF activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP316594.RAvgFg37G47rl8uYY66XsiVsX0a1BaCE_hGRHClP-VCdc130_assertion description "[Exon deletion in the non-catalytic domain of eIF2Bepsilon due to a splice site mutation leads to infantile forms of CACH/VWM with severe decrease of eIF2B GEF activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316594.RAvgFg37G47rl8uYY66XsiVsX0a1BaCE_hGRHClP-VCdc130_provenance.
- NP831794.RAuobUHjNO6abAsDEDxTfBY0lzpp3QsiPl2zKj3E2LSLw130_assertion description "[Exon deletion in the non-catalytic domain of eIF2Bepsilon due to a splice site mutation leads to infantile forms of CACH/VWM with severe decrease of eIF2B GEF activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831794.RAuobUHjNO6abAsDEDxTfBY0lzpp3QsiPl2zKj3E2LSLw130_provenance.