Mutation in KCNQ1 that has both recessive and dominant characteristics

Journal of Medical Genetics

Volumn 39, Issue 9, 2002, Pages 681-685

  Murray, A ^a   Potet, F ^b   Bellocq, C ^b   Baro I ^b   Reardon, W ^c   Hughes, H E ^d   Jeffery, S ^a  

^a ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

^b HÔTEL DIEU   (France)

^c National Centre for Medical Genetics   (Ireland)

^d UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA;

ADOLESCENT; ANIMAL CELL; ARTICLE; CASE REPORT; CELL STRAIN COS7; CLINICAL FEATURE; DIAGNOSTIC VALUE; DOMINANT INHERITANCE; ELECTROPHYSIOLOGY; FAMILIAL DISEASE; FEMALE; GENE MUTATION; GENETIC ANALYSIS; HEARING IMPAIRMENT; HEART ARREST; HETEROZYGOTE; HUMAN; LONG QT SYNDROME; MALE; NONHUMAN; PLASMID; PRIORITY JOURNAL; QT INTERVAL; RECESSIVE INHERITANCE;

ANIMALIA;

EID: 0036711619     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.39.9.681     Document Type: Article

References (26)

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