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Volumn 59, Issue 2, 2005, Pages 51-56

G6PD deficiency in Vataliya Prajapati community settled in Surat

Author keywords

Chronic hemolytic anemia; G6PD deficiency; G6PD enzyme activity; Hemolytic crisis; Vataliya Prajapati

Indexed keywords

GLUCOSE 6 PHOSPHATE DEHYDROGENASE;

EID: 22144441655     PISSN: 00195359     EISSN: None     Source Type: Journal    
DOI: 10.4103/0019-5359.13903     Document Type: Article
Times cited : (11)

References (12)
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  • 2
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    • A single mutation is responsible for the high prevalence of G6PD deficiency in Vataliya Prajapati -An endogamous caste group from western India
    • Sukumar S, Colah B, Mohanty D, Joshi SR. A single mutation is responsible for the high prevalence of G6PD deficiency in Vataliya Prajapati -An endogamous caste group from western India. Am J Hematol 2001;67:218-9.
    • (2001) Am J Hematol , vol.67 , pp. 218-219
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    • Glader BE, Lukens IN. Glucose-6-phosphate dehydrogenase deficiency and related disorders of hexose monophosphate shunt and glutathiche metaboligms. In "Wintrobe's clinical hematology" editors: Lukens J, Paraskavas P, Greer JP, Roger GM, X edition volume I, Baltimore: Willams & Wilking company; 1998. p. 1176-90.
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    • Genetical diseases other than hemoglobinopathies in India
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.