Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D

American Journal of Human Genetics

Volumn 63, Issue 6, 1998, Pages 1622-1630

  Honsho, Masanori ^a,b   Tamura, Shigehiko ^a   Shimozawa, Nobuyuki ^c   Suzuki, Yasuyuki ^c   Kondo, Naomi ^c   Fujiki, Yukio ^a,b  

^a KYUSHU UNIVERSITY   (Japan)

^b JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

^c GIFU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CONTROLLED STUDY; GENE MUTATION; GENETIC LINKAGE; HUMAN; HUMAN CELL; NUCLEOTIDE SEQUENCE; PEROXISOME; PRIORITY JOURNAL; PROTEIN EXPRESSION; SKIN FIBROBLAST; ZELLWEGER SYNDROME;

YARROWIA LIPOLYTICA;

EID: 0032471611     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302161     Document Type: Article

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