1.
Merchant ZN, Gosai MM, Kaklotar JH, Shah AP. Siblings with nemaline myopathy: a case of rare genetic mutation. Int J Contemp Pediatr [Internet]. 2024 Nov. 25 [cited 2026 May 21];11(12):1822-5. Available from: https://www.ijpediatrics.com/index.php/ijcp/article/view/6339