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pro vyhledávání: '"Sandip P Bartakke"'
Autor:
Reema Garegrat, Suprabha K Patnaik, Nandini Malshe, Sandip P Bartakke, Vibha Bafna, Pradeep Suryawanshi
Publikováno v:
Indian Pediatrics Case Reports, Vol 2, Iss 2, Pp 102-106 (2022)
Background: Clinical, pathologic, and genetic heterogeneity is a challenge in identifying and classifying congenital dyserythropoietic anemia (CDA). CDA type IV, the rarest CDA with only 11 reported cases, results from KLF1 gene mutation. Clinical De
Externí odkaz:
https://doaj.org/article/82cc355ccee442459f9b69f5fb26bf42