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Functional impact of the head domain variants of DES (Desmin) on filament assembly.
Voß S, Walhorn V, Holler S, Gärtner A, Pohl G, Tiesmeier J, Gummert J, Anselmetti D, Milting H, Brodehl A. Voß S, et al. Among authors: brodehl a. Genes Dis. 2024 Feb 2;12(1):101238. doi: 10.1016/j.gendis.2024.101238. eCollection 2025 Jan. Genes Dis. 2024. PMID: 39650696 Free PMC article. No abstract available.
A novel desmin (DES) indel mutation causes severe atypical cardiomyopathy in combination with atrioventricular block and skeletal myopathy.
Schirmer I, Dieding M, Klauke B, Brodehl A, Gaertner-Rommel A, Walhorn V, Gummert J, Schulz U, Paluszkiewicz L, Anselmetti D, Milting H. Schirmer I, et al. Among authors: brodehl a. Mol Genet Genomic Med. 2018 Mar;6(2):288-293. doi: 10.1002/mgg3.358. Epub 2017 Dec 23. Mol Genet Genomic Med. 2018. PMID: 29274115 Free PMC article.
The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy.
Kulikova O, Brodehl A, Kiseleva A, Myasnikov R, Meshkov A, Stanasiuk C, Gärtner A, Divashuk M, Sotnikova E, Koretskiy S, Kharlap M, Kozlova V, Mershina E, Pilus P, Sinitsyn V, Milting H, Boytsov S, Drapkina O. Kulikova O, et al. Among authors: brodehl a. Genes (Basel). 2021 Jan 19;12(1):121. doi: 10.3390/genes12010121. Genes (Basel). 2021. PMID: 33478057 Free PMC article.
Special Issue "Cardiovascular Genetics".
Brodehl A, Milting H, Gerull B. Brodehl A, et al. Genes (Basel). 2021 Mar 26;12(4):479. doi: 10.3390/genes12040479. Genes (Basel). 2021. PMID: 33810227 Free PMC article.
52 results