1.
Barp A, Neri LM, Maggi L, Iascone M, Gualandi F. A novel deep intronic mutation expands the genotype spectrum of MYH7-related myopathies. Acta Myol [Internet]. 2025 Sep. 30 [cited 2025 Oct. 6];44(3). Available from: https://www.actamyologica.it/article/view/1282