Additional file 2 of Chromatinopathies: clinically overlapping disorders, revealing novel variants and their DNA methylation signatures
Asuman Koparir(University of Würzburg), E Klopocki(University of Würzburg), Erkan Koparir(University of Würzburg), Jessica Rzasa(London Health Sciences Centre), Yvonne Jelting(Universitätsklinikum Würzburg), Wahyu Eka Prastyo(University of Würzburg), Jonas Deinlein(University of Würzburg), Nicole Stachelscheid(Klinikum Aschaffenburg), Jörg Klepper(Klinikum Aschaffenburg), Thomas König(Universitätsklinikum Würzburg), Eva Metzger(Genetikum), Neda Dragicevic Babic(Universitätsklinikum Würzburg), Paulina Bahena Carbajal(Universitätsmedizin Rostock), Bekim Sadikovic(Western University), Erdmute Kunstmann(University of Würzburg), Eva Runkel(Klinikum Aschaffenburg), Jennifer Kerkhof(London Health Sciences Centre), Thomas Haaf(University of Würzburg), Michaela A. H. Hofrichter(University of Würzburg), Konstantinos Kolokotronis(University of Zurich), Juliane Spiegler(Universitätsklinikum Würzburg)
Cited by 0
Related Papers
<scp>DFNB16</scp> is a frequent cause of congenital hearing impairment: implementation of <i><scp>STRC</scp></i> mutation analysis in routine diagnostics
|Clinical Genetics|2013|110
Non-syndromic hearing loss gene identification: A brief history and glimpse into the future
|Molecular and Cellular Probes|2015|109
Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations
|Genetics in Medicine|2014|107
Small fish, big prospects: using zebrafish to unravel the mechanisms of hereditary hearing loss
|Hearing Research|2020|33
Confirmation of PDZD7 as a Nonsyndromic Hearing Loss Gene
|Ear and Hearing|2016|29