Identification and functional characterization of the first deep intronic GLA mutation (IVS4+1326C>T) causing renal variant of Fabry disease

Overview of attention for article published in Orphanet Journal of Rare Diseases, June 2022

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Identification and functional characterization of the first deep intronic GLA mutation (IVS4+1326C>T) causing renal variant of Fabry disease https://t.co/GZf8dyt432

21 Jun 2022

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