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Volumn 7, Issue 1, 1996, Pages 1-6

Mutations in pyruvate kinase

Author keywords

Anemia; Glucocerebrosidase; NSHA; Pyruvate kinase

Indexed keywords

COMPLEMENTARY DNA; GLUCOSYLCERAMIDASE; PYRUVATE KINASE;

EID: 0030030548     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1996)7:1<1::AID-HUMU1>3.0.CO;2-H     Document Type: Review
Times cited : (23)

References (18)
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  • 2
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    • Analysis of pyruvate kinase (PK) mutations that produce nonspherocytic hemolytic anemia
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  • 3
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    • Prenatal diagnosis of pyruvate kinase deficiency
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  • 4
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    • Molecular study of pyruvate kinase deficient patients affected by nonspherocytic hemolytic anemia
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    • Baronciani, L.1    Beutler, E.2
  • 5
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  • 7
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    • Elevated pyruvate kinase activity in patients with hemolytic anemia due to red cell pyruvate kinase "deficiency"
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    • Beutler, E.1    Forman, L.2    Rios-Larrain, E.3
  • 8
    • 0003236185 scopus 로고
    • Molecular characterization of L-PK gene in pyruvate kinase (PK) deficient Italian patients
    • Bianchi P, Terragna C, Zappa M, Alfinito F, Zanella A (1994) Molecular characterization of L-PK gene in pyruvate kinase (PK) deficient Italian patients. Blood 84:14a.
    • (1994) Blood , vol.84
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  • 10
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  • 12
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    • Glenn, D.1    Gelbart, T.2    Beutler, E.3
  • 13
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  • 14
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  • 15
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    • 384→Met) affecting enzymatic stability in a pyruvate kinase variant (PK Tokyo) associated with hereditary hemolytic anemia. Proc Natl Acad Sci USA 88:8218-8221.
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  • 17
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.