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Genetic heterogeneity of peroxisome biogenesis disorders among Japanese patients: Evidence for a founder haplotype for the most commonPEX10 gene mutation

✍ Scribed by Shimozawa, Nobuyuki ;Nagase, Tomoko ;Takemoto, Yasuhiko ;Ohura, Toshihiro ;Suzuki, Yasuyuki ;Kondo, Naomi


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
79 KB
Volume
120A
Category
Article
ISSN
0148-7299

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