Ibrahim, A.; Sharathkumar, A.; McLaughlin, H.; Claassen, D.; Bhagavathi, S.
Congenital Neutropenia with Specific Granulocyte Deficiency Caused by Novel Double Heterozygous SMARCD2 Mutations. Hematol. Rep. 2022, 14, 270-275.
https://doi.org/10.3390/hematolrep14030038
AMA Style
Ibrahim A, Sharathkumar A, McLaughlin H, Claassen D, Bhagavathi S.
Congenital Neutropenia with Specific Granulocyte Deficiency Caused by Novel Double Heterozygous SMARCD2 Mutations. Hematology Reports. 2022; 14(3):270-275.
https://doi.org/10.3390/hematolrep14030038
Chicago/Turabian Style
Ibrahim, Abukhiran, Anjali Sharathkumar, Heather McLaughlin, David Claassen, and Sharathkumar Bhagavathi.
2022. "Congenital Neutropenia with Specific Granulocyte Deficiency Caused by Novel Double Heterozygous SMARCD2 Mutations" Hematology Reports 14, no. 3: 270-275.
https://doi.org/10.3390/hematolrep14030038
APA Style
Ibrahim, A., Sharathkumar, A., McLaughlin, H., Claassen, D., & Bhagavathi, S.
(2022). Congenital Neutropenia with Specific Granulocyte Deficiency Caused by Novel Double Heterozygous SMARCD2 Mutations. Hematology Reports, 14(3), 270-275.
https://doi.org/10.3390/hematolrep14030038