Corrigendum to "Severe cardiac phenotype of Berardinelli-Seip congenital lipodystrophy in an infant with a E158X BSCL2 mutation" [Eur. J. Med. Genet. 52 (1) (2009) 14-16] (DOI:10.1016/j.ejmg.2008.10.006);Severe cardiac phenotype of Berardinelli-Seip congenital lipodystrophy in an infant with homozygous E189X BSCL2 mutation

European Journal of Medical Genetics

Volumn 52, Issue 1, 2009, Pages 14-16

  Friguls, B ^a   Coroleu, W ^a   del Alcazar, R ^a   Hilbert, P ^b   Van Maldergem, L ^b   Pintos Morell, G ^a  

^a UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^b INSTITUTE OF PATHOLOGY AND GENETICS   (Belgium)

Author keywords

Berardinelli Seip congenital lipodystrophy; Hypertrophic cardiomyopathy; Insulin resistance; Leptin

Indexed keywords

PROPRANOLOL;

ARTICLE; BSCL2 GENE; CASE REPORT; CONGENITAL GENERALIZED LIPODYSTROPHY; DIET THERAPY; GENE; GENE MUTATION; GENETIC ANALYSIS; HEART FAILURE; HOMOZYGOSITY; HUMAN; HYPERGLYCEMIA; HYPERINSULINEMIA; HYPERTENSION; HYPERTROPHIC CARDIOMYOPATHY; INFANT; MALE; PANCREATITIS; PARENTERAL NUTRITION; PHENOTYPE; STOP CODON;

EID: 58149117493     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2009.03.008     Document Type: Erratum

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