POLG1 mutations manifesting as autosomal recessive axonal Charcot-Marie-Tooth disease.
Harrower T; Stewart JD; Hudson G; Houlden H; Warner G; O'Donovan DG; Findlay LJ; Taylor RW; De Silva R; Chinnery PF; Archives Of Neurology, 2008, vol. 65, issue 1, p 133, ISSN 00039942. ISBN 00039942.

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