Mucopolysaccharidosis type I: Characterization of a common mutation that causes Hurler syndrome in Moroccan subjects

Annals of Human Genetics

Volumn 63, Issue 1, 1999, Pages 9-16

  Alif, N ^a   Hess, Ketsia ^b,d   Straczek, J ^b   Sebbar, S ^c   N'Bou, A ^c   Nabet, P ^b   Dousset, B ^b  

^a IBN ZOHR UNIVERSITY   (Morocco)

^b School of Medicine   (France)

^c HASSAN II UNIVERSITY HOSPITAL   (Morocco)

^d UNIVERSITÉ DE LORRAINE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

LEVO IDURONIDASE;

ADOLESCENT; ADULT; ARTICLE; BASE MISPAIRING; CHILD; CLINICAL ARTICLE; EUROPE; FAMILY; FEMALE; FLUORESCENCE ANALYSIS; GENE MUTATION; GENETIC SCREENING; GEOGRAPHIC DISTRIBUTION; HUMAN; HUMAN CELL; HURLER SYNDROME; MALE; MOROCCO; MUCOPOLYSACCHARIDOSIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SIBLING; TWINS;

ADOLESCENT; ADULT; ALLELES; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; FEMALE; HUMANS; IDURONIDASE; MALE; MOROCCO; MUCOPOLYSACCHARIDOSIS I; MUTATION, MISSENSE; PHENOTYPE; POINT MUTATION;

EID: 0032766994     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0003480099007344     Document Type: Article

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