Matches in Nanopublications for { ?s ?p "[Mutations of the novel renal glomerular genes NPHS1 and NPHS2 encoding nephrin and podocin cause two types of severe nephrotic syndrome presenting in early life, Finnish type congenital nephrotic syndrome (CNF) and a form of autosomal recessive familial focal segmental glomerulosclerosis (SRN1), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_assertion description "[Mutations of the novel renal glomerular genes NPHS1 and NPHS2 encoding nephrin and podocin cause two types of severe nephrotic syndrome presenting in early life, Finnish type congenital nephrotic syndrome (CNF) and a form of autosomal recessive familial focal segmental glomerulosclerosis (SRN1), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_provenance.
- NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_assertion description "[Mutations of the novel renal glomerular genes NPHS1 and NPHS2 encoding nephrin and podocin cause two types of severe nephrotic syndrome presenting in early life, Finnish type congenital nephrotic syndrome (CNF) and a form of autosomal recessive familial focal segmental glomerulosclerosis (SRN1), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_provenance.