Associated Papers
[MPIG6B gene variation causing thrombocytopenia with myelofibrosis in a child].
Wang Y et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2025
MPIG6B Gene-Related Myelofibrosis: A Rare Inherited Disease That Is Frequently Described in Arab Population.
Attar LJ et al.
Avicenna Journal of Medicine, 2024
A novel MPIG6B gene mutation in an adolescent girl with congenital thrombocytopenia and myelofibrosis.
Wang Z et al.
Current Research in Translational Medicine, 2022
ASXL2 mutated myelodysplastic syndrome in a novel germline G6b variant.
Qu S et al.
Leukemia Research Reports, 2022
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