KFU. Card publication. A familial case of MYH9 gene mutation associated with impaired platelet functionality and structural alterations.

KAZAN
FEDERAL UNIVERSITY

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A FAMILIAL CASE OF MYH9 GENE MUTATION ASSOCIATED WITH IMPAIRED PLATELET FUNCTIONALITY AND STRUCTURAL ALTERATIONS.

Form of presentation

Conference proceedings in international journals and collections

Year of publication

2022

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Authors, employees of KFU

Daminova Amina Galeevna, author

Evtyugina Natalya Gennadevna, author

Kravcova Olga Aleksandrovna, author

Litvinov Rustem Igorevich, author

Peshkova Alina Dmitrievna, author

Safiullina Svetlana Ildarovna, author

Khabirova Alina Ilshatovna, author

Khismatullin Rafael Rafikovich, author

Authors, postgraduates KFU

Evtyugina Natalya Gennadevna, postgraduate kfu

Bibliographic description in the original language

S. I. Safiullina, N. G. Evtugina, R. R. Khismatullin, O. A. Kravtsova, A. I. Khabirova, C. Nagaswami, I. A. Andrianova, A. G. Daminova, A. D. Peshkova, J. W. Weisel, R. I. Litvinov. A familial case of MYH9 gene mutation associated with impaired platelet functionality and structural alterations. Research and Practice in Thrombosis and Haemostasis; 2022; 6 (Suppl 1). Abstract: PB1239. https://doi.org/10.1002/rth2.12788

Annotation

Research and Practice in Thrombosis and Haemostasis

Keywords

MYH9 gene mutation, platelets

The name of the journal

Research and Practice in Thrombosis and Haemostasis

URL

https://doi.org/10.1002/rth2.12788

Please use this ID to quote from or refer to the card

https://repository.kpfu.ru/eng/?p_id=275166&p_lang=2

Full metadata record

Field DC	Value	Language
dc.contributor.author	Daminova Amina Galeevna	ru_RU
dc.contributor.author	Evtyugina Natalya Gennadevna	ru_RU
dc.contributor.author	Kravcova Olga Aleksandrovna	ru_RU
dc.contributor.author	Litvinov Rustem Igorevich	ru_RU
dc.contributor.author	Peshkova Alina Dmitrievna	ru_RU
dc.contributor.author	Safiullina Svetlana Ildarovna	ru_RU
dc.contributor.author	Khabirova Alina Ilshatovna	ru_RU
dc.contributor.author	Khismatullin Rafael Rafikovich	ru_RU
dc.contributor.author	Evtyugina Natalya Gennadevna	ru_RU
dc.date.accessioned	2022-01-01T00:00:00Z	ru_RU
dc.date.available	2022-01-01T00:00:00Z	ru_RU
dc.date.issued	2022	ru_RU
dc.identifier.citation	S. I. Safiullina, N. G. Evtugina, R. R. Khismatullin, O. A. Kravtsova, A. I. Khabirova, C. Nagaswami, I. A. Andrianova, A. G. Daminova, A. D. Peshkova, J. W. Weisel, R. I. Litvinov. A familial case of MYH9 gene mutation associated with impaired platelet functionality and structural alterations. Research and Practice in Thrombosis and Haemostasis; 2022; 6 (Suppl 1). Abstract: PB1239. https://doi.org/10.1002/rth2.12788	ru_RU
dc.identifier.uri	https://repository.kpfu.ru/eng/?p_id=275166&p_lang=2	ru_RU
dc.description.abstract	Research and Practice in Thrombosis and Haemostasis	ru_RU
dc.language.iso	ru	ru_RU
dc.subject	MYH9 gene mutation	ru_RU
dc.subject	platelets	ru_RU
dc.title	A familial case of MYH9 gene mutation associated with impaired platelet functionality and structural alterations.	ru_RU
dc.type	Conference proceedings in international journals and collections	ru_RU