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Volumn 26, Issue 7, 2006, Pages
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Analysis of ankyrin-B gene mutations in patients with long QT syndrome.
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Author keywords
[No Author keywords available]
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Indexed keywords
ANK2 PROTEIN, HUMAN;
ANKYRIN;
ADOLESCENT;
ADULT;
AGED;
AMINO ACID SUBSTITUTION;
ARTICLE;
CHILD;
EXON;
FEMALE;
GENETICS;
HUMAN;
LONG QT SYNDROME;
MALE;
MIDDLE AGED;
MISSENSE MUTATION;
MOLECULAR GENETICS;
NUCLEOTIDE SEQUENCE;
POINT MUTATION;
PRESCHOOL CHILD;
ADOLESCENT;
ADULT;
AGED;
AGED, 80 AND OVER;
AMINO ACID SUBSTITUTION;
ANKYRINS;
BASE SEQUENCE;
CHILD;
CHILD, PRESCHOOL;
EXONS;
FEMALE;
HUMANS;
LONG QT SYNDROME;
MALE;
MIDDLE AGED;
MOLECULAR SEQUENCE DATA;
MUTATION, MISSENSE;
POINT MUTATION;
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EID: 42449129350
PISSN: 16734254
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (2)
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References (0)
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