Latest Nanopublications by Núria Queralt Rosinach

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 NGLY1 deficiency is a novel autosomal recessive disorder of the ERAD pathway. SuperPatternInstance

 Dysfunction of ERAD pathway Class

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 RA_Oxu-sQ9

 NGLY1 deficiency is a novel autosomal recessive disorder of the ERAD pathway. SuperPatternInstance

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