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Variability of disease progression in a family with autosomal recessive CMT associated with a S194X and new R310Q mutation in the GDAP1 gene

✍ Scribed by H Azzedine; M Ruberg; D Ente; C Gilardeau; S Périé; B Wechsler; A Brice; E LeGuern; O Dubourg

No coin nor oath required. For personal study only.

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