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Novel SLFN14 mutation associated with macrothrombocytopenia in a patient with severe haemorrhagic syndrome

Document Type

Letter

Author

Polokhov, D.; Fedorova, D.; Ignatova, A.; Ponomarenko, E.; Rashevskaya, E.; Martyanov, A.; Podoplelova, N.; Aleksenko, M.; Mersiyanova, I.; Seregina, E.; Poletaev, A.; Truchina, E.; Raykina, E.; Plyasunova, S.; Novichkova, G.; Zharkov, P.; Panteleev, M.

Source

In: Orphanet Journal of Rare Diseases. (Orphanet Journal of Rare Diseases, December 2023, 18(1))

Subject

Language

English

ISSN

17501172

Online Access

EBSCOHost PDF Full Text (ProQuest Central) Full Text (Gale Academic Onefile) Open Access (BioMed Central) Web of Science JCR 저널정보 Scopus Find it@PNU

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