Yüklüyor......

A PCR-SSP method for detecting the His63Asp mutation in the HFE gene associated with hereditary haemochromatosis.

Hereditary haemochromatosis is an autosomal recessive disease in which there is defective regulation of iron absorption, causing gradual accumulation of excessive amounts of iron in certain organs. Recently, a candidate gene for hereditary haemochromatosis has been identified, located on the short a...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yazar: Smillie, D
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1998
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC395644/
https://ncbi.nlm.nih.gov/pubmed/9893753
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!