On the edge of noncompaction: Minimally manifesting Duchenne carrier due to the dystrophin mutation n.2867A>C

International Journal of Cardiology

Volumn 165, Issue 2, 2013, Pages

  Finsterer, Josef ^a   Stöllberger, Claudia ^a   Vlckova, Zoja ^b   Gencik, Martin ^b  

^a KRANKENANSTALT RUDOLFSTIFTUNG   (Austria)

^b Human Genetic Laboratory   (Austria)

Author keywords

Duchenne; Dystorphin; Hypertrabeculation; Non compaction; Noncompaction; Point mutation

Indexed keywords

ADENINE; CREATINE KINASE; CYTOSINE; DYSTROPHIN; MYOGLOBIN; AMINO TERMINAL PRO BRAIN NATRIURETIC PEPTIDE; BISOPROLOL;

ADULT; CASE REPORT; CLINICAL FEATURE; CONGESTIVE CARDIOMYOPATHY; DISEASE CARRIER; DUCHENNE MUSCULAR DYSTROPHY; ELECTROCARDIOGRAPHY; ETHNIC GROUP; FAMILY HISTORY; FEMALE; GENE MUTATION; HUMAN; LETTER; MUSCLE CRAMP; MUSCLE WEAKNESS; NERVE CONDUCTION; NEUROLOGIC EXAMINATION; POINT MUTATION; PRIORITY JOURNAL; VENTRICULAR NONCOMPACTION; VIETNAMESE; AMINO ACID SUBSTITUTION; BECKER MUSCULAR DYSTROPHY; DYSTROPHIN GENE; ECG ABNORMALITY; ECHOCARDIOGRAPHY; FOLLOW UP; HEART RIGHT BUNDLE BRANCH BLOCK; HEART VENTRICLE EXTRASYSTOLE; SINUS BRADYCARDIA; SINUS TACHYCARDIA; YOUNG ADULT;

EID: 84876668531     PISSN: 01675273     EISSN: 18741754     Source Type: Journal    
DOI: 10.1016/j.ijcard.2012.10.075     Document Type: Article

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