Carrier frequency of SMN1‐related spinal muscular atrophy in north Indian population: The need for population based screening program - Nilay, Mayank; Moirangthem, Amita; Saxena, Deepti; Mandal, Kausik; Phadke, Shubha R. (American journal of medical genetics. Part A, 2021)
Keywords: Catchment areas; Chromosome 5; Exons; Gene deletion; Hereditary diseases; Infant mortality; Neuromuscular diseases; SMN protein; Spinal muscular atrophy