–
Статьи в журналах
-
- 2021 Hemi- and homozygous loss-of-function mutations in DSG2 (Desmoglein-2) cause recessive arrhythmogenic cardiomyopathy with an early onset
- Brodehl Andreas, Meshkov Alexey, Myasnikov Roman, Kiseleva Anna, Kulikova Olga, Klauke Bärbel, Sotnikova Evgeniia, Stanasiuk Caroline, Divashuk Mikhail, Pohl Greta Marie, Kudryavtseva Maria, Klingel Karin, Gerull Brenda, Zharikova Anastasia, Gummert Jan, Koretskiy Sergey, Schubert Stephan, Mershina Elena, Gärtner Anna, Pilus Polina, Laser Kai Thorsten, Sinitsyn Valentin, Boytsov Sergey, Drapkina Oxana, Milting Hendrik
- в журнале International Journal of Molecular Sciences, издательство MDPI (Basel, Switzerland), том 22, № 7, с. 1-15 DOI