Novel functional mutations of the galactosidase alpha (GLA) gene in Fabry disease-Reference-Cited by-同舟云学术

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Novel functional mutations of the galactosidase alpha (GLA) gene in Fabry disease

Published:2024-08-01 Issue:8 Volume:117 Page:551-551
ISSN:1460-2725
Container-title:QJM: An International Journal of Medicine
language:en
Short-container-title:

Author:

Donnelly Seamas C¹

Affiliation:

1. QJM Editor-in-Chief,

Publisher

Oxford University Press (OUP)

Link

https://academic.oup.com/qjmed/article-pdf/117/8/551/59089677/hcae151.pdf

Reference5 articles.

1. Adult-onset leigh’s syndrome: a rare cause of young-onset parkinsonism with dystonia;Saluja;QJM,2024

2. A novel compound heterozygous mutation in the SLC34A2 gene causes pulmonary alveolar microlithiasis;Liu;QJM,2024

3. SARS-CoV-2-associated Guillain-Barré syndrome is a Para-infectious disease;Li;QJM,2021

4. The evolving spectrum of human african trypanosomiasis;Kennedy;QJM,2024

5. IgG4-related pericarditis;Son;QJM,2024

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