Reghis, Abderrezak

Top Publications

Top Publications Authored or Co-Authored by "Reghis, Abderrezak"

• Primary adhalinopathy: A common cause of autosomal recessive muscular dystrophy of variable severity

  Nature Genetics, Volume 10, No. 2, Year 1995, Citations 197
• Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kda dystrophin-associated glycoprotein maps to chromosome 13q12

  Human Molecular Genetics, Volume 2, No. 9, Year 1993, Citations 94
• Characterization of two novel splice site mutations in human factor VII gene causing severe plasma factor VII deficiency and bleeding diathesis

  British Journal of Haematology, Volume 117, No. 1, Year 2002, Citations 58
• G6pD aures: A new mutation (48 lle → Thr) causing mild G6PD deficiency is associated with favism

  Human Molecular Genetics, Volume 2, No. 1, Year 1993, Citations 34
• At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria

  Human Genetics, Volume 94, No. 5, Year 1994, Citations 31