Work

Gaucher disease type 3: Variability in phenotype among siblings with same mutation

Year: 2020

Type: article

Study design: Observational Study

Source: Molecular Genetics and Metabolism

DOI: 10.1016/j.ymgme.2019.11.120

Authors: Fatma T. Eminoglu, Ummühan Öncül

Institution: Ankara University

Language: English

Topic: Lysosomal Storage Disorders Research

Subfield: Physiology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W3003622739

FWCI:

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