Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B

Human Molecular Genetics

Volumn 7, Issue 9, 1998, Pages 1399-1405

  Okumoto, Kanji ^a   Itoh, Ryota ^a   Shimozawa, Nobuyuki ^b   Suzuki, Yasuyuki ^b   Tamura, Shigehiko ^a   Kondo, Naomi ^b   Fujiki, Yukio ^a,c  

^a KYUSHU UNIVERSITY   (Japan)

^b GIFU UNIVERSITY   (Japan)

^c JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; ZINC FINGER PROTEIN;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BIOGENESIS; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; CYTOSOL; DISORDERS OF PEROXISOMAL FUNCTIONS; DNA LIBRARY; FIBROBLAST; FRAMESHIFT MUTATION; GENE MUTATION; GENETIC COMPLEMENTATION; HANSENULA POLYMORPHA; HUMAN; HUMAN CELL; LIVER; NONHUMAN; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; ZELLWEGER SYNDROME;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CHO CELLS; CLONING, MOLECULAR; CRICETINAE; DNA, COMPLEMENTARY; FUNGAL PROTEINS; GENE EXPRESSION; GENETIC COMPLEMENTATION TEST; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; OLIGONUCLEOTIDE PROBES; PHEX PHOSPHATE REGULATING NEUTRAL ENDOPEPTIDASE; PICHIA; PROTEINS; SEQUENCE HOMOLOGY, AMINO ACID; TRANSFECTION; ZELLWEGER SYNDROME;

ANIMALIA; PICHIA ANGUSTA;

EID: 0031656796     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/7.9.1399     Document Type: Article

References (38)

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