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Gaucher Disease Type 1, A Rare Disease: A Single Center-Experience
Author(s) -
Fatma İlknur Varol,
Ayşe Selimoğlu,
Şükrü Güngör,
Bengü Macit
Publication year - 2021
Publication title -
journal of contemporary medicine
Language(s) - Uncategorized
Resource type - Journals
ISSN - 2667-7180
DOI - 10.16899/jcm.807622
Subject(s) - medicine , enzyme replacement therapy , organomegaly , hepatosplenomegaly , abdominal pain , disease , glucocerebrosidase , pediatrics , glucocerebroside , lysosomal storage disease , rare disease , cytopenia , abdomen , physical examination , surgery , bone marrow

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