[1]
Myathari, R., Gupta, A. and Bijarnia-Mahay, S. 2022. Novel mutation in DMN1L gene in child with Landau Kleffner syndrome: a rare association. International Journal of Contemporary Pediatrics. 9, 9 (Aug. 2022), 855–859. DOI:https://doi.org/10.18203/2349-3291.ijcp20222127.