Concepedia

Mutation in Is Causal in the Peroxisome-Deficient Zellweger Syndrome of Complementation Group D

Masanori Honsho, Shigehiko Tamura, Nobuyuki Shimozawa, Yasuyuki Suzuki, Naomi Kondo, Yukio Fujiki

The American Journal of Human Genetics · 1998 · 169 citations · 43 references

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43

Basic local alignment search tool

Stephen F. Altschul, Warren Gish, Webb Miller et al. · Journal of Molecular Biology · 1990 · 94.5K citations

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The Metabolic Basis of Inherited Disease.

Annals of Internal Medicine · 1988 · 7.8K citations

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The metabolic basis of inherited disease

JL Goldstein · Medical Entomology and Zoology · 1995 · 1K citations

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A novel, cleavable peroxisomal targeting signal at the amino‐terminus of the rat 3‐ketoacyl‐CoA thiolase.

Bart W. Swinkels, Stephen J. Gould, Andrea Bodnár et al. · The EMBO Journal · 1991 · 626 citations · Full text

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Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata

Nancy Braverman, Gary Steel, Cassandra Obie et al. · Nature Genetics · 1997 · 445 citations

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