Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome

Circulation

Volumn 99, Issue 10, 1999, Pages 1344-1347

  Chen, Qiuyun ^a   Zhang, Danmei ^a   Gingell, Robert L ^b   Moss, Arthur J ^c   Napolitano, Carlo ^d,e   Priori, Silvia G ^d,e   Schwartz, Peter J ^d,e   Kehoe, Eileen ^c   Robinson, Jennifer L ^c   Schulze Bahr, Eric ^f   Wang, Qing ^a   Towbin, Jeffrey A ^a,g  

^a TEXAS CHILDREN S HOSPITAL   (United States)

^b CHILDREN S HOSPITAL OF BUFFALO   (United States)

^c UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

^d UNIVERSITY OF PAVIA   (Italy)

^e FONDAZIONE IRCCS POLICLINICO SAN MATTEO   (Italy)

^f UNIVERSITY HOSPITAL MÜNSTER   (Germany)

^g BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

Deafness; Jervell and Lange Nielsen syndrome; Long QT syndrome; Potassium channel

Indexed keywords

POTASSIUM; POTASSIUM CHANNEL;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL RECESSIVE DISORDER; CLINICAL FEATURE; CONTROLLED STUDY; DELETION MUTANT; DNA POLYMORPHISM; FRAMESHIFT MUTATION; GENE MUTATION; HEARING IMPAIRMENT; HETEROZYGOTE; HOMOZYGOSITY; HUMAN; HUMAN CELL; LONG QT SYNDROME; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

EID: 0033574219     PISSN: 00097322     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.CIR.99.10.1344     Document Type: Article

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