Literature DB >> 8490627

G6PD Aures: a new mutation (48 Ile-->Thr) causing mild G6PD deficiency is associated with favism.

K Nafa1, A Reghis, N Osmani, L Baghli, M Benabadji, J C Kaplan, T J Vulliamy, L Luzzatto.   

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Year:  1993        PMID： 8490627     DOI： 10.1093/hmg/2.1.81

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN： 0964-6906            Impact factor:   6.150


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  8 in total

1.  Path to facilitate the prediction of functional amino acid substitutions in red blood cell disorders--a computational approach.

Authors:  Rajith B; George Priya Doss C
Journal:  PLoS One       Date:  2011-09-13       Impact factor: 3.240

2.  Glucose-6-phosphate dehydrogenase variants associated with favism in Thai children.

Authors:  Vichai Laosombat; Benjamas Sattayasevana; Teerachit Chotsampancharoen; Malai Wongchanchailert
Journal:  Int J Hematol       Date:  2006-02       Impact factor: 2.490

3.  At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria.

Authors:  K Nafa; A Reghis; N Osmani; L Baghli; H Aït-Abbes; M Benabadji; J C Kaplan; T Vulliamy; L Luzzatto
Journal:  Hum Genet       Date:  1994-11       Impact factor: 4.132

4.  Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Jeddah, Kingdom of Saudi Arabia.

Authors:  Soad K Al-Jaouni; Jummanah Jarullah; Essam Azhar; Kamran Moradkhani
Journal:  BMC Res Notes       Date:  2011-10-24

5.  Molecular characterization of glucose-6-phosphate dehydrogenase deficient variants in Baghdad city - Iraq.

Authors:  Bassam Ms Al-Musawi; Nasir Al-Allawi; Ban A Abdul-Majeed; Adil A Eissa; Jaladet Ms Jubrael; Hanan Hamamy
Journal:  BMC Blood Disord       Date:  2012-03-27

Review 6.  Arab gene geography: From population diversities to personalized medical genomics.

Authors:  Ghazi O Tadmouri; Konduru S Sastry; Lotfi Chouchane
Journal:  Glob Cardiol Sci Pract       Date:  2014-12-31

7.  Molecular characterization of G6PD mutations reveals the high frequency of G6PD Aures in the Lao Theung population.

Authors:  Amkha Sanephonasa; Chalisa Louicharoen Cheepsunthorn; Naly Khaminsou; Onekham Savongsy; Issarang Nuchprayoon; Kamonlak Leecharoenkiat
Journal:  Malar J       Date:  2021-01-07       Impact factor: 2.979

8.  Genotype-Phenotype Correlation of G6PD Mutations among Central Thai Children with G6PD Deficiency.

Authors:  Boonchai Boonyawat; Tim Phetthong; Nithipun Suksumek; Chanchai Traivaree
Journal:  Anemia       Date:  2021-02-09
  8 in total

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