학술논문
Hemi‐ and homozygous loss‐of‐function mutations in dsg2 (Desmoglein‐2) cause recessive arrhythmogenic cardiomyopathy with an early onset
Document Type
Article
Author
Brodehl, A.; Klauke, B.; Stanasiuk, C.; Pohl, G.M.; Gummert, J.; Gärtner, A.; Milting, H.; Meshkov, A.; Myasnikov, R.; Kiseleva, A.; Kulikova, O.; Sotnikova, E.; Divashuk, M.; Kudryavtseva, M.; Zharikova, A.; Koretskiy, S.; Drapkina, O.; Klingel, K.; Gerull, B.; Schubert, S.; Laser, K.T.; Mershina, E.; Pilus, P.; Sinitsyn, V.; Boytsov, S.
Source
In: International Journal of Molecular Sciences . (International Journal of Molecular Sciences, 1 April 2021, 22(7))
Subject
Language
English
ISSN
14220067
16616596
16616596