Illuminating Friedreich's Ataxia

17 June 2019

By Dr Nicola Davies

This month we delve into the diagnosis and treatment of Friedreich’s Ataxia (FA), a rare inherited genetic disorder affecting approximately one to two people per 50,000.1,2 Pharma’s role in advancing the care of these patients is also explored by Dr Nicola Davies in her exclusive series for The Pharma Letter.

What is Friedreich’s Ataxia?

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