Matches in Nanopublications for { ?s ?p "[Mutations in the specific delta-aminolevulinic acid synthase (ALAS) 2 isoform that catalyses the first and rate-limiting step in heme synthesis pathway in the mitochondrial matrix, lead to ineffective erythropoiesis that characterizes X-linked sideroblastic anemia (XLSA), the most common inherited sideroblastic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 2 of
2
with 100 items per page.
- NP8268.RA9lVRJe4fI0IdszVcTQoj6GEWva_pe69jSi33J3kpf7M130_assertion description "[Mutations in the specific delta-aminolevulinic acid synthase (ALAS) 2 isoform that catalyses the first and rate-limiting step in heme synthesis pathway in the mitochondrial matrix, lead to ineffective erythropoiesis that characterizes X-linked sideroblastic anemia (XLSA), the most common inherited sideroblastic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8268.RA9lVRJe4fI0IdszVcTQoj6GEWva_pe69jSi33J3kpf7M130_provenance.
- NP6497.RAIAcqnzWXA49Jebx18FFXD6t01x0O9pP9Ykp2g0lTSTU130_assertion description "[Mutations in the specific delta-aminolevulinic acid synthase (ALAS) 2 isoform that catalyses the first and rate-limiting step in heme synthesis pathway in the mitochondrial matrix, lead to ineffective erythropoiesis that characterizes X-linked sideroblastic anemia (XLSA), the most common inherited sideroblastic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6497.RAIAcqnzWXA49Jebx18FFXD6t01x0O9pP9Ykp2g0lTSTU130_provenance.