Identification of two novel missense mutations causing severe factor XIII deficiency.
| Data(s) |
01/05/2015
|
|---|---|
| Formato |
application/pdf |
| Identificador |
http://boris.unibe.ch/81595/1/V.Schroeder_H.Handrkova_hae12663.pdf Handrková, Helena; Borhany, M; Schröder, Verena; Fatima, N; Hussain, A; Shamsi, T; Kohler, H P (2015). Identification of two novel missense mutations causing severe factor XIII deficiency. Haemophilia, 21(3), e253-e256. Blackwell Science 10.1111/hae.12663 <http://dx.doi.org/10.1111/hae.12663> doi:10.7892/boris.81595 info:doi:10.1111/hae.12663 info:pmid:25832324 urn:issn:1351-8216 |
| Idioma(s) |
eng |
| Publicador |
Blackwell Science |
| Relação |
http://boris.unibe.ch/81595/ |
| Direitos |
info:eu-repo/semantics/restrictedAccess |
| Fonte |
Handrková, Helena; Borhany, M; Schröder, Verena; Fatima, N; Hussain, A; Shamsi, T; Kohler, H P (2015). Identification of two novel missense mutations causing severe factor XIII deficiency. Haemophilia, 21(3), e253-e256. Blackwell Science 10.1111/hae.12663 <http://dx.doi.org/10.1111/hae.12663> |
| Palavras-Chave | #610 Medicine & health |
| Tipo |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion PeerReviewed |
