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searching for PEX13 2 found (16 total)

alternate case: pEX13

Infantile Refsum disease (866 words) [view diff] exact match in snippet view article find links to article

(2006). "Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients". Human Mutation. 27 (11): 1157. doi:10.1002/humu

PEX12 (1,168 words) [view diff] case mismatch in snippet view article find links to article

Mano S, Nakamori C, Nito K, et al. (2007). "The Arabidopsis pex12 and pex13 mutants are defective in both PTS1- and PTS2-dependent protein transport