Loading Filters
Showing 1–3 of 3 results
-
Research | | Open
Autosomal recessive cardiomyopathy and sudden cardiac death associated with variants in MYL3
- homa.tajsharghi@his.se
- Daniel Peter Sayer Osborn
- , Leila Emrahi
- , Joshua Clayton
- , Mehrnoush Toufan Tabrizi
- , Alex Yui Bong Wan
- , Reza Maroofian
- , Mohammad Yazdchi
- , Michael Leon Enrique Garcia
- , Hamid Galehdari
- , Camila Hesse
- , Gholamreza Shariati
- , Neda Mazaheri
- , Alireza Sedaghat
- , Hayley Goullée
- , Nigel Laing
- , Yalda Jamshidi
- & Homa Tajsharghi
-
Research |
Mutations and sequence variation in the human myosin heavy chain IIa gene (MYH2)
- homa.tajsharghi@pathology.gu.se
-
Research |
Recessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutations
- homa.tajsharghi@gu.se
