Analysis of a 43.6 kb deletion in a patient with Hunter syndrome (MPSII): Identification of a fusion transcript including sequences from the gene W and the IDS gene

Human Mutation

Volumn 15, Issue 4, 2000, Pages 324-331

  Lagerstedt, K ^a   Carlberg, B M ^a   Karimi Nejad, R ^b   Kleijer, W J ^c   Bondeson, M L ^a  

^a UPPSALA UNIVERSITY   (Sweden)

^b Karimi Nejad Pathology and Genetic Center   (Iran)

^c ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

Hunter syndrome; IDS; Illegitimate recombination; MPSII

Indexed keywords

ALTERNATIVE RNA SPLICING; ARTICLE; CASE REPORT; CHILD; DNA SEQUENCE; FUSION GENE; GENE DELETION; GENE EXPRESSION; GENE SEQUENCE; GENETIC RECOMBINATION; HUMAN; HUNTER SYNDROME; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS;

ALTERNATIVE SPLICING; BASE COMPOSITION; BASE SEQUENCE; CHILD; HUMANS; IDURONATE SULFATASE; INFANT, NEWBORN; MALE; MOLECULAR SEQUENCE DATA; MUCOPOLYSACCHARIDOSIS II; RECOMBINATION, GENETIC; SEQUENCE DELETION;

EID: 0034113706     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(200004)15:4<324::AID-HUMU4>3.0.CO;2-5     Document Type: Article

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