KFU. Card publication. A familial case of MYH9 gene mutation associated with multiple functional and structural platelet abnormalities.

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FEDERAL UNIVERSITY

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A FAMILIAL CASE OF MYH9 GENE MUTATION ASSOCIATED WITH MULTIPLE FUNCTIONAL AND STRUCTURAL PLATELET ABNORMALITIES.

Form of presentation

Articles in international journals and collections

Year of publication

2022

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Authors, employees of KFU

Andrianova Izabella Aleksandrovna, author

Evtyugina Natalya Gennadevna, author

Kravcova Olga Aleksandrovna, 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

Khismatullin Rafael Rafikovich, postgraduate kfu

Bibliographic description in the original language

S. I. Safiullina, N. G. Evtugina, I. A. Andrianova, R. R. Khismatullin, O. A. Kravtsova, A. I. Khabirova, C. Nagaswami, A. G. Aminova, A. D. Peshkova, R. I. Litvinov, J. W. Weisel. A familial case of MYH9 gene mutation associated with multiple functional and structural platelet abnormalities. Scientific Reports, 2022, 12:19975.

Keywords

MYH9 gene, MYH9-related disorders, platelets

The name of the journal

SCIENTIFIC REPORTS

URL

https://doi.org/10.1038/s41598-022-24098-5

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

https://repository.kpfu.ru/eng/?p_id=275163&p_lang=2

Resource files

File name	Size (MB)	Format
F_Scientific_Reports_2022___MY_9.pdf	3,45	pdf	show / download

Full metadata record

Field DC	Value	Language
dc.contributor.author	Andrianova Izabella Aleksandrovna	ru_RU
dc.contributor.author	Evtyugina Natalya Gennadevna	ru_RU
dc.contributor.author	Kravcova Olga Aleksandrovna	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.contributor.author	Khismatullin Rafael Rafikovich	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, I. A. Andrianova, R. R. Khismatullin, O. A. Kravtsova, A. I. Khabirova, C. Nagaswami, A. G. Aminova, A. D. Peshkova, R. I. Litvinov, J. W. Weisel. A familial case of MYH9 gene mutation associated with multiple functional and structural platelet abnormalities. Scientific Reports, 2022, 12:19975.	ru_RU
dc.identifier.uri	https://repository.kpfu.ru/eng/?p_id=275163&p_lang=2	ru_RU
dc.description.abstract	SCIENTIFIC REPORTS	ru_RU
dc.language.iso	ru	ru_RU
dc.subject	MYH9 gene	ru_RU
dc.subject	MYH9-related disorders	ru_RU
dc.subject	platelets	ru_RU
dc.title	A familial case of MYH9 gene mutation associated with multiple functional and structural platelet abnormalities.	ru_RU
dc.type	Articles in international journals and collections	ru_RU