The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading

Background:Patients with hereditary haemochromatosis (HH) are usually homozygous for the C282Y mutation in the HFE gene. They have variable expression of iron overload and present with a variety of complications, including liver disease, diabetes, arthropathy, fatigue, and cardiomyopathy. The mitoch...

Полное описание

Сохранить в:
Библиографические подробности
Главные авторы: Livesey, K, Wimhurst, V, Carter, K, Worwood, M, Cadet, E, Rochette, J, Roberts, A, Pointon, J, Merryweather-Clar..., A, Bassett, M, Jouanolle, A, Mosser, A, David, V, Poulton, J, Robson, K
Формат: Artigo
Язык:Inglês
Опубликовано: BMJ Group 2004
Предметы:
Original Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC1757237/
https://ncbi.nlm.nih.gov/pubmed/14729817
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2003.008805
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Схожие документы