Robert Hufnagel to Charcot-Marie-Tooth Disease
This is a "connection" page, showing publications Robert Hufnagel has written about Charcot-Marie-Tooth Disease.
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Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder. Nat Genet. 2015 Aug; 47(8):926-32.
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