Novel GLA T194A variant causes Fabry disease

Maria Nicole Pestana1, Francisca Gomes da Silva2, José Durães2

  • 1Nephrology, Hospital Doctor Nélio Mendonça, Funchal, Portugal nicole.pest@gmail.com.

BMJ Case Reports
|March 2, 2021
PubMed
Summary

A novel Fabry disease mutation in the GLA gene was identified in a woman and her children. This finding expands understanding of Fabry disease genetics and its variable clinical presentation.

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