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Journal Articles

Congenital Erythrocytosis Due to Novel CMTR1 K769L Mutation Has Augmented Hypoxia Signaling and Features of Both Primary and Secondary Erythrocytosis

Jihyun Song, Lorenzo D. Botto, Beverly Schaefer, Soo Jin Kim, Tatiana Tvrdik, Rong Mao, Undiagnosed Diseases Network (UDN), Josef T. Prchal

Blood (2022) 140 (Supplement 1): 1243–1244.

https://doi.org/10.1182/blood-2022-167863

Published: 2022