CODE Think! Rare Mutations of STX3 Causing Microvillus Inclusion Disease
代码思考!STX3 的罕见突变导致微绒毛包涵体病
期刊:Journal of Pediatric Genetics
影响因子:0.4
doi:10.1055/s-0043-1772207
John, Elizabeth Mary; Sathyan, Sajina; Pournami, Femitha; Prithvi, Ajai Kumar; Nandakumar, Anand; Prabhakar, Jyothi; Jain, Naveen