Phenotypes of myopathy-related beta-tropomyosin mutants in human and mouse tissue cultures.

by Saba Abdul-Hussein, Karin Rahl, Ali-Reza Moslemi, Homa Tajsharghi
Published 2013-01-01

Developmental MYH3 Myopathy Associated with Expression of Mutant Protein and Reduced Expression Levels of Embryonic MyHC.

by Malgorzata Pokrzywa, Michaela Norum, Johan Lengqvist, Mehrnaz Ghobadpour, Saba Abdul-Hussein, Ali-Reza Moslemi, Homa Tajsharghi
Published 2015-01-01

Motor neuron diseases caused by a novel VRK1 variant – A genotype/phenotype study

by Maryam Sedghi, Ali‐Reza Moslemi, Montse Olive, Masoud Etemadifar, Behnaz Ansari, Jafar Nasiri, Leila Emrahi, Hamid‐Reza Mianesaz, Nigel G. Laing, Homa Tajsharghi
Published 2019-11-01