Tuba Hilkay Karapınar
0000-0002-4714-332X
2 papers found
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Cerebral Involvement of Hemophagocytic Lymphohistiocytosis in Griscelli Syndrome
Homozygous c.130–131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry
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