Funder
Interdisziplinäres Zentrum für Klinische Forschung, Universitätsklinikum Würzburg
BMBF Berlin
Deutsche Forschungsgemeinschaft
Julius-Maximilians-Universität Würzburg
Bundesministerium für Bildung und Forschung
Subject
Cell Biology,Molecular Biology
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2. Cardiac features of a novel autosomal recessive dilated cardiomyopathic syndrome due to defective importation of mitochondrial protein;Sparkes;Cardiol Young,2007
3. New mutation of mitochondrial DNAJC19 causing dilated and noncompaction cardiomyopathy, anemia, ataxia, and male genital anomalies;Ojala;Pediatr Res,2012
4. Progressive cerebellar atrophy and a novel homozygous pathogenic DNAJC19 variant as a cause of dilated cardiomyopathy ataxia syndrome;Al Teneiji;Pediatr Neurol,2016
5. Previously unreported biallelic mutation in DNAJC19: are sensorineural hearing loss and basal Ganglia Lesions additional features of dilated cardiomyopathy and ataxia (DCMA) syndrome?;Ucar;JIMD Rep,2017
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