Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies - Semmler, Anna-Lena; Müller, Oliver J. (BioMed Central, 2016)
Gesehen am 16.02.2016
Aus: Orphanet Journal of Rare Diseases, 9 (2014), Nr. 121. pp. 1-13. ISSN 1750-1172