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Volumn 2012, Issue , 2012, Pages 13-18
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Gaucher disease and other storage disorders.
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Author keywords
[No Author keywords available]
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Indexed keywords
CERAMIDE;
ADOLESCENT;
ADULT;
APOPTOSIS;
BIOLOGICAL MODEL;
CHEMICAL MODEL;
CHEMISTRY;
ENZYME THERAPY;
FEMALE;
GAUCHER DISEASE;
GENOTYPE;
HEMATOLOGY;
HUMAN;
LYSOSOME;
LYSOSOME STORAGE DISEASE;
MALE;
METABOLISM;
METHODOLOGY;
MOLECULAR BIOLOGY;
PHENOTYPE;
REVIEW;
TREATMENT OUTCOME;
ADOLESCENT;
ADULT;
APOPTOSIS;
CERAMIDES;
ENZYME THERAPY;
FEMALE;
GAUCHER DISEASE;
GENOTYPE;
HEMATOLOGY;
HUMANS;
LYSOSOMAL STORAGE DISEASES;
LYSOSOMES;
MALE;
MODELS, BIOLOGICAL;
MODELS, CHEMICAL;
MOLECULAR BIOLOGY;
PHENOTYPE;
TREATMENT OUTCOME;
MLCS;
MLOWN;
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EID: 84878475101
PISSN: None
EISSN: 15204383
Source Type: Journal
DOI: 10.1182/asheducation.v2012.1.13.3797921 Document Type: Review |
Times cited : (99)
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References (0)
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