Phenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disorders

American Journal of Human Genetics

Volumn 63, Issue 5, 1998, Pages 1294-1306

  Chang, Chia Che ^a   Gould, Stephen J ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BIOGENESIS; CLINICAL ARTICLE; CONTROLLED STUDY; GENE SEQUENCE; GENOTYPE; HUMAN; HUMAN CELL; INBORN ERROR OF METABOLISM; MENTAL DEFICIENCY; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PEROXISOME; PHENOTYPE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; ZELLWEGER SYNDROME;

EID: 0032231622     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302103     Document Type: Article

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