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Identification and characterization of novel mutations implicated in congenital fibrinogen disorders

Document Type

Article

Author

Smith, N.; Noetzli, L.; Jacobson, L.; White-Adams, T.C.; Manco-Johnson, M.; Di Paola, J.; Bornikova, L.; Guglielmone, H.; Minoldo, S.; Backos, D.S.; Thornburg, C.D.; Escobar, M.; Wolberg, A.S.

Source

In: Research and Practice in Thrombosis and Haemostasis. (Research and Practice in Thrombosis and Haemostasis, October 2018, 2(4):800-811)

Subject

Language

English

ISSN

24750379

Online Access

Full Text (ScienceDirect 종량제) Full Text (Clinical Key) Full Text (ProQuest Central) Full Text (ScienceDirect O/A) Web of Science JCR 저널정보 Scopus Find it@PNU

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