Search Results - "Hoyer, L.W."

Haemophilia A: database of ncleotide substituttions, deletions, insertions and rearrangements of the factor VIII gene by Tuddenham, E.G.D., Cooper, D.N., Gitschier, J., Higuchi, M., Hoyer, L.W., Yoshioka, A., Peake, I.R., Schwaab, R., Olek, K., Kazazian, H.H., Lavergne, J.M., Giannelli, F., Antonarakis, S.E.

Get full text

Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition by Tuddenham, E.G.D., Schwaab, R., Seehafer, J., Millar, D.S., Gitschier, J., Higuchi, M., Bidichandani, S., Connor, J.M., Hoyer, L.W., Yoshioka, A., Peake, I.R., Olek, K., Kazazian, H.H., Lavergne, J.-M., Giannelli, F., Antonarakis, S.E., Cooper, D.N.

“…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…”
Get full text

Spectrum of mutations in CRM-positive and CRM-reduced hemophilia A by McGinniss, M J, Kazazian, Jr, H H, Hoyer, L W, Bi, L, Inaba, H, Antonarakis, S E

“…Hemophilia A is due to the functional deficiency of factor VII (FVIII, gene locus F8C). Although half the patients have no detectable FVIII protein in their…”
Get more information

Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition by Tuddenham, E.G.D., Schwaab, R., Seehafer, J., Millar, D.S., Gitschier, J., Higuchi, M., Bidichandani, S., Connor, J.M., Hoyer, L.W., Yoshioka, A., Peake, I.R., Olek, K., Kazazian, H.H., Lavergne, J.-M., Giannelli, F., Antonarakis, S.E., Cooper, D.N.

“…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…”
Get full text