Matches in Nanopublications for { ?s ?p "[This study provides the first evidence for a homozygous missense mutation in SCN5A and suggests that LQTS with functional 2:1 AVB in young children, a severe phenotype associated with bad prognosis, may be caused by homozygous or heterozygous compound mutations not only in HERG but also in SCN5A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP500958.RAG0qHv8vu2PNJ_RKbQv3LLl8oa28271o8x8BBheGMkxc130_assertion description "[This study provides the first evidence for a homozygous missense mutation in SCN5A and suggests that LQTS with functional 2:1 AVB in young children, a severe phenotype associated with bad prognosis, may be caused by homozygous or heterozygous compound mutations not only in HERG but also in SCN5A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500958.RAG0qHv8vu2PNJ_RKbQv3LLl8oa28271o8x8BBheGMkxc130_provenance.
- assertion description "[This study provides the first evidence for a homozygous missense mutation in SCN5A and suggests that LQTS with functional 2:1 AVB in young children, a severe phenotype associated with bad prognosis, may be caused by homozygous or heterozygous compound mutations not only in HERG but also in SCN5A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[This study provides the first evidence for a homozygous missense mutation in SCN5A and suggests that LQTS with functional 2:1 AVB in young children, a severe phenotype associated with bad prognosis, may be caused by homozygous or heterozygous compound mutations not only in HERG but also in SCN5A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP324538.RAQ8YX1hkh7mXBHffUKY4xkqUzcE6ifXEauvSPrpPI264130_assertion description "[This study provides the first evidence for a homozygous missense mutation in SCN5A and suggests that LQTS with functional 2:1 AVB in young children, a severe phenotype associated with bad prognosis, may be caused by homozygous or heterozygous compound mutations not only in HERG but also in SCN5A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324538.RAQ8YX1hkh7mXBHffUKY4xkqUzcE6ifXEauvSPrpPI264130_provenance.
- NP521727.RA0WjPBZqdgWGUpgUHfz00kFfkpC3iiyN6kI0c3-I6yyk130_assertion description "[This study provides the first evidence for a homozygous missense mutation in SCN5A and suggests that LQTS with functional 2:1 AVB in young children, a severe phenotype associated with bad prognosis, may be caused by homozygous or heterozygous compound mutations not only in HERG but also in SCN5A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521727.RA0WjPBZqdgWGUpgUHfz00kFfkpC3iiyN6kI0c3-I6yyk130_provenance.
- NP324537.RA-x7V7pyahjuVR-WPGOcDlJMHzK9HMGRxnDvdx9q7tfs130_assertion description "[This study provides the first evidence for a homozygous missense mutation in SCN5A and suggests that LQTS with functional 2:1 AVB in young children, a severe phenotype associated with bad prognosis, may be caused by homozygous or heterozygous compound mutations not only in HERG but also in SCN5A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324537.RA-x7V7pyahjuVR-WPGOcDlJMHzK9HMGRxnDvdx9q7tfs130_provenance.