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Article

Platelet functional abnormalities and clinical presentation in pediatric patients with germline RUNX1, ANKRD26, and ETV6 mutations.

Haematologica - 1 Oct 2022

Ovsyannikova Galina S, Fedorova Daria V, Tesakov Ivan P, Martyanov Alexey A, Ignatova Anastasia A, Ponomarenko Evgeniya A, Zharkov Pavel A, Pavlova Anna V, Raykina Elena V, Maschan Michael A, Panteleev Mikhail A, Novichkova Galina A, Sveshnikova Anastasia N, Smetanina Nataliya S

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Share to Blood Platelet Disorders
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 35796010
DOI: 10.3324/haematol.2022.281340
PMCID: PMC9521247

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