Matches in Nanopublications for { ?s ?p "[A novel INF2 mutation in a Korean family with autosomal dominant intermediate Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP7875.RAUW2F-bdbeU-cGFBzCZ-CuK2IQ3dlMJqivt7X6VdZQvg130_assertion description "[A novel INF2 mutation in a Korean family with autosomal dominant intermediate Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7875.RAUW2F-bdbeU-cGFBzCZ-CuK2IQ3dlMJqivt7X6VdZQvg130_provenance.
- assertion description "[A novel INF2 mutation in a Korean family with autosomal dominant intermediate Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A novel INF2 mutation in a Korean family with autosomal dominant intermediate Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1175273.RArAsfXFkh0l4gsq5r6uPfpDdKSQHRKCjSqqcW-P0hnx0130_assertion description "[A novel INF2 mutation in a Korean family with autosomal dominant intermediate Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1175273.RArAsfXFkh0l4gsq5r6uPfpDdKSQHRKCjSqqcW-P0hnx0130_provenance.
- NP1175274.RA9Iv2mupckP3VpR24OJrjS4IEuRC6jq_QTvar5N--fSY130_assertion description "[A novel INF2 mutation in a Korean family with autosomal dominant intermediate Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1175274.RA9Iv2mupckP3VpR24OJrjS4IEuRC6jq_QTvar5N--fSY130_provenance.