Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition.

A large number of different mutations in the factor VIII (F8) gene have been identified as a cause of haemophilia A. This compilation lists known single base-pair substitutions, deletions and insertions in the F8 gene and reviews the status of the inversional events which account for a substantial p...

Descripció completa

Dades bibliogràfiques

Publicat a:	Nucleic Acids Res
Autors principals:	Tuddenham, E G, Schwaab, R, Seehafer, J, Millar, D S, Gitschier, J, Higuchi, M, Bidichandani, S, Connor, J M, Hoyer, L W, Yoshioka, A
Format:	Artigo
Idioma:	Inglês
Publicat:	Oxford University Press 1994
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC308545/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7984443/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/22.22.4851
Etiquetes:	Afegir etiqueta Sense etiquetes, Sigues el primer a etiquetar aquest registre!