Biochemical properties of β-glucosidase in leukocytes from patients and obligated heterozygotes for Gaucher disease carriers

Clinica Chimica Acta

Volumn 362, Issue 1-2, 2005, Pages 101-109

  Michelin, Kristiane ^a,b   Wajner, Alessandro ^a,b   Bock, Hugo ^a   Fachel, Ângela ^a   Rosenberg, Roberto ^c   Flores Pires, Ricardo ^a   Saraiva Pereira, Maria Luiza ^a,b   Giugliani, Roberto ^a,b   Coelho, Janice Carneiro ^a,b  

^a HOSPITAL DE CLÍNICAS DE PORTO ALEGRE   (Brazil)

^b FEDERAL UNIVERSITY OF RIO GRANDE DO SUL   (Brazil)

^c UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Glucosidase; Gaucher's disease; Lysosomal storage diseases; Sphingolipidosis

Indexed keywords

BETA GLUCOSIDASE;

ANALYTIC METHOD; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE CARRIER; ENZYME ANALYSIS; ENZYME INACTIVATION; ENZYME STABILITY; GAUCHER DISEASE; GENE MUTATION; GENOTYPE; HETEROZYGOTE; HUMAN; HUMAN CELL; INCUBATION TEMPERATURE; INCUBATION TIME; LEUKOCYTE; PH MEASUREMENT; PRIORITY JOURNAL; THERMOSTABILITY;

BETA-GLUCOSIDASE; ENZYME STABILITY; GAUCHER DISEASE; HEAT; HETEROZYGOTE; HUMANS; HYDROGEN-ION CONCENTRATION; LEUKOCYTES; MUTATION; PROTEIN DENATURATION;

EID: 27744558023     PISSN: 00098981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cccn.2005.06.010     Document Type: Article

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