← Evidence map

ArticleMolecular genetics and metabolism reports2021

New mutation in Fabry disease: c.448delG, first phenotypic description.

Esteban Calabrese et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

2 papers cite it

2021
2022
2023
2024
2025
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 33732617