Search Results - "Mason, N G"

Molecular epidemiology of erythropoietic protoporphyria in the U.K by Whatley, S.D., Mason, N.G., Holme, S.A., Anstey, A.V., Elder, G.H., Badminton, M.N.

“…Summary Background  Erythropoietic protoporphyria (EPP) is a cutaneous porphyria caused by mutations in the ferrochelatase (FECH) or, less frequently, the…”
Get full text

Autosomal recessive erythropoietic protoporphyria in the United Kingdom: prevalence and relationship to liver disease by Whatley, S D, Mason, N G, Khan, M, Zamiri, M, Badminton, M N, Missaoui, W N, Dailey, T A, Dailey, H A, Douglas, W S, Wainwright, N J, Elder, G H

“…6- 10 Most individuals who are heterozygous for these mutations are asymptomatic, despite having half-normal FECH activities. 11 For protoporphyrin to…”
Get full text

Ferrochelatase gene polymorphism analysis for accurate genetic counselling in erythropoietic protoporphyria by Morris, S.D., Mason, N.G., Elder, G.H., Hawk, J.L.M., Sarkany, R.P.E.

“…Summary It has recently been shown that most cases of clinically overt erythropoietic protoporphyria (EPP) result from coinheritance of a mutated…”
Get full text

Points: A limited role for manipulation? by Mason, G N G

Get full text

A Limited Role For Manipulation? by Mason, G. N. G.

Get full text