MERCHANT, Z. N.; GOSAI, M. M.; KAKLOTAR, J. H.; SHAH, A. P. Siblings with nemaline myopathy: a case of rare genetic mutation. International Journal of Contemporary Pediatrics, [S. l.], v. 11, n. 12, p. 1822–1825, 2024. DOI: 10.18203/2349-3291.ijcp20243486. Disponível em: https://www.ijpediatrics.com/index.php/ijcp/article/view/6339. Acesso em: 21 may. 2026.