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Volumn 46, Issue 5, 2001, Pages 273-277

The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6

(9) Matsumoto, N a,b Tamura, S a Moser, A c Moser, H W c Braverman, N d Suzuki, Y e Shimozawa, N e Kondo, N e Fujiki, Y a,b

a KYUSHU UNIVERSITY (Japan)

b JAPAN SCIENCE AND TECHNOLOGY AGENCY (Japan)

c JOHNS HOPKINS UNIVERSITY (United States)

d JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE (United States)

e GIFU UNIVERSITY (Japan)

Author keywords

AAA ATPase; Complementation groups; Peroxin; Peroxisomal biogenesis disorders; PEX6; Protein import

Indexed keywords

PEROXIN;

ALLELE; ARTICLE; DISORDERS OF PEROXISOMAL FUNCTIONS; FIBROBLAST; GENE EXPRESSION; GENETIC COMPLEMENTATION; HUMAN; HUMAN CELL; NUCLEOTIDE SEQUENCE; PEROXISOME; ZELLWEGER SYNDROME;

ADENOSINE TRIPHOSPHATASES; AMINO ACID SEQUENCE; CELL FUSION; CELL LINE; CLONING, MOLECULAR; DNA MUTATIONAL ANALYSIS; DNA, COMPLEMENTARY; FIBROBLASTS; GENETIC COMPLEMENTATION TEST; HUMANS; MOLECULAR SEQUENCE DATA; PEROXISOMAL DISORDERS; PEROXISOMES; TRANSFECTION;

EID: 0035052383 PISSN: 14345161 EISSN: None Source Type: Journal
DOI: 10.1007/s100380170078 Document Type: Article

Times cited : (33)

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