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

Mutations at the factor VIII gene locus causing Haemophilia A have now been identified in many patients from many ethnic groups. Earlier studies used biased methods which detected repetitive mutations at a few CG dinucleotides. More recently rapid gene scanning methods have uncovered an extreme dive...

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Dades bibliogràfiques

Publicat a:	Nucleic Acids Res
Autors principals:	Tuddenham, E G, Cooper, D N, Gitschier, J, Higuchi, M, Hoyer, L W, Yoshioka, A, Peake, I R, Schwaab, R, Olek, K, Kazazian, H H
Format:	Artigo
Idioma:	Inglês
Publicat:	Oxford University Press 1991
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC328775/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1923751/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/19.18.4821
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