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...

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Podrobná bibliografie

Vydáno v:	Nucleic Acids Res
Hlavní autoři:	Tuddenham, E G, Schwaab, R, Seehafer, J, Millar, D S, Gitschier, J, Higuchi, M, Bidichandani, S, Connor, J M, Hoyer, L W, Yoshioka, A
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Oxford University Press 1994
On-line přístup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC308313/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7937051/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/22.17.3511
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