Andersen syndrome autosomal dominant in three generations

American Journal of Medical Genetics

Volumn 85, Issue 2, 1999, Pages 147-156

  Canún, Sonia ^a   Pérez, Nohemí ^a   Beirana, Luisa G ^b  

^a HOSPITAL GENERAL DR MANUEL GEA GONZÁLEZ   (Mexico)

^b HOSPITAL DE PEDIATRÍA   (Mexico)

Author keywords

Andersen syndrome; Long QT; Periodic paralysis; Pierre Robin like; Sudden death

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CLINICAL ARTICLE; FEMALE; GENE EXPRESSION; GENETIC DISORDER; HEART VENTRICLE ARRHYTHMIA; HUMAN; LONG QT SYNDROME; MALE; PERIODIC PARALYSIS; PRIORITY JOURNAL; SUDDEN DEATH; SYNCOPE;

ADOLESCENT; ADULT; ARRHYTHMIA; CHILD; DEATH, SUDDEN; FACE; FACIES; FEMALE; GENES, DOMINANT; HUMANS; MALE; PARALYSES, FAMILIAL PERIODIC; PEDIGREE; POTASSIUM; SYNCOPE; SYNDROME;

EID: 0345620973     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990716)85:2<147::AID-AJMG9>3.0.CO;2-0     Document Type: Article

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