Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.
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H. Moser | A. Moser | N. Shimozawa | S. Tamura | Yasuyuki Suzuki | Y. Fujiki | N. Kondo | Non Miyata | N. Matsumoto | Satomi Furuki