Literature DB >> 9354698

A cheaper and more rapid polymerase chain reaction-restriction fragment length polymorphism method for the detection of the HLA-H gene mutations occurring in hereditary hemochromatosis.

C Lynas.   

Abstract

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Year:  1997        PMID： 9354698

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  5 in total

1.  Frequencies of HFE gene mutations associated with haemochromatosis in the population of Libya living in Benghazi.

Authors:  Samir Elmrghni; Ron A Dixon; D Ross Williams
Journal:  Int J Clin Exp Med       Date:  2011-09-15

2.  Prevalence of HFE mutations and relation to serum iron status in patients with chronic hepatitis C and patients with nonalcoholic fatty liver disease in Taiwan.

Authors:  Tsung-Jung Lin; Chih-Lin Lin; Chaur-Shine Wang; Shu-O Liu; Li-Ying Liao
Journal:  World J Gastroenterol       Date:  2005-07-07       Impact factor: 5.742

3.  Simultaneous detection of C282Y and H63D hemochromatosis mutations by dual-color probes.

Authors:  M Phillips; C A Meadows; M Y Huang; A Millson; E Lyon
Journal:  Mol Diagn       Date:  2000-06

4.  Homogeneous multiplex genotyping of hemochromatosis mutations with fluorescent hybridization probes.

Authors:  P S Bernard; R S Ajioka; J P Kushner; C T Wittwer
Journal:  Am J Pathol       Date:  1998-10       Impact factor: 4.307

5.  Association of frequency of hereditary hemochromatosis (HFE) gene mutations (H63D and C282Y) with iron overload in beta-thalassemia major patients in Pakistan.

Authors:  Yasir Sharif; Saba Irshad; Anam Tariq; Sana Rasheed; Muhammad H Tariq
Journal:  Saudi Med J       Date:  2019-09       Impact factor: 1.484
  5 in total

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