Matches in Nanopublications for { ?s ?p "[We have searched for mutations in the maleylacetoacetate isomerase gene in four cases of unexplained severe liver failure in infancy with clinical similarities to hereditary tyrosinemia type I (pseudotyrosinemia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP616075.RABBzSvksKzyUUY-rseBcjdzV2D60ym5FLo_4H7mQzdhU130_assertion description "[We have searched for mutations in the maleylacetoacetate isomerase gene in four cases of unexplained severe liver failure in infancy with clinical similarities to hereditary tyrosinemia type I (pseudotyrosinemia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616075.RABBzSvksKzyUUY-rseBcjdzV2D60ym5FLo_4H7mQzdhU130_provenance.
- NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_assertion description "[We have searched for mutations in the maleylacetoacetate isomerase gene in four cases of unexplained severe liver failure in infancy with clinical similarities to hereditary tyrosinemia type I (pseudotyrosinemia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_provenance.
- NP441138.RADXTJlIZYWwFmve_mMoVgbN8IHqrS8dv5qyxRY7bfMoI130_assertion description "[We have searched for mutations in the maleylacetoacetate isomerase gene in four cases of unexplained severe liver failure in infancy with clinical similarities to hereditary tyrosinemia type I (pseudotyrosinemia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441138.RADXTJlIZYWwFmve_mMoVgbN8IHqrS8dv5qyxRY7bfMoI130_provenance.
- NP441140.RAF3p3bLqSgw0OnAVxBy8nLBBXxQSCd_x-XR8Rs_RsHcU130_assertion description "[We have searched for mutations in the maleylacetoacetate isomerase gene in four cases of unexplained severe liver failure in infancy with clinical similarities to hereditary tyrosinemia type I (pseudotyrosinemia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441140.RAF3p3bLqSgw0OnAVxBy8nLBBXxQSCd_x-XR8Rs_RsHcU130_provenance.
- NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_assertion description "[We have searched for mutations in the maleylacetoacetate isomerase gene in four cases of unexplained severe liver failure in infancy with clinical similarities to hereditary tyrosinemia type I (pseudotyrosinemia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_provenance.
- NP255338.RA8iqCk-0rPtMKzUOuzzWwndUkAF2eqEqlLVgiwXp2t_A130_assertion description "[We have searched for mutations in the maleylacetoacetate isomerase gene in four cases of unexplained severe liver failure in infancy with clinical similarities to hereditary tyrosinemia type I (pseudotyrosinemia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP255338.RA8iqCk-0rPtMKzUOuzzWwndUkAF2eqEqlLVgiwXp2t_A130_provenance.