2019. May
De novo mutations in COL4A5 identified by whole exome sequencing in 2 girls with Alport syndrome in Korea.
Korean J Pediatr. 2019
Han KH, Park JE, Ki CS.
De novo mutations in COL4A5 identified by whole exome sequencing in 2 girls with Alport syndrome in Korea.
Korean J Pediatr. 2019
Han KH, Park JE, Ki CS.