Incidence of peroxisomal disorders in Japan

Japanese Journal of Human Genetics

Volumn 41, Issue 1, 1996, Pages 167-175

  Suzuki, Yasuyuki ^a,b   Shimozawa, Nobuyuki ^a   Yajima, Shigehiro ^a   Inoue, Kyoko ^a   Orii, Tadao ^a   Kondo, Naomi ^a  

^a GIFU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b Chubu Women's College   (Japan)

Author keywords

complementation group; peroxisomal disorders; screening; very long chain fatty acid(s)

Indexed keywords

ACYL COENZYME A OXIDASE; SPHINGOMYELIN; VERY LONG CHAIN FATTY ACID;

ADOLESCENT; ADRENOLEUKODYSTROPHY; ARTICLE; CHILD; CHONDRODYSPLASIA PUNCTATA; DISORDERS OF PEROXISOMAL FUNCTIONS; ENZYME DEFICIENCY; FATTY ACID SYNTHESIS; FEMALE; GENETIC COUNSELING; HUMAN; HUMAN CELL; HUMAN TISSUE; INFANT; JAPAN; LIPIDOSIS; MAJOR CLINICAL STUDY; MALE; NEWBORN; ZELLWEGER SYNDROME;

EID: 0029983106     PISSN: 09168478     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF01892624     Document Type: Article

References (18)

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