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Gaucher disease and β-thalassemia: A rare coinheritance.

Blood cells, molecules & diseases - 1 Jun 2017

Makis Alexandros, Tzoufi Meropi, Pappa Eleni, Kyrochristos Ioannis, Zikou Anastasia, Xydis Vasileios, Argyropoulou Maria I, Chaliasos Nikolaos

Abstract excerpt

No abstract is available from the source.

Topics

Child
Enzyme Replacement Therapy
Gaucher Disease
Glucosylceramidase
Hepatomegaly
Humans
Magnetic Resonance Imaging
Male
Mutation
Paternal Inheritance
Splenomegaly
beta-Globins
beta-Thalassemia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 28458077
DOI: 10.1016/j.bcmd.2017.04.007

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