Development of a mnemonic screening tool for identifying subjects with Hunter syndrome

European Journal of Pediatrics

Volumn 172, Issue 7, 2013, Pages 965-970

  Cohn, Gabriel M ^a   Morin, Isabelle ^b   Whiteman, David A H ^a  

^a Shire Human Genetic Therapies Inc   (United States)

^b Shire Human Genetic Therapies ^*  (Switzerland)

Author keywords

Diagnosis; Hunter syndrome; Lysosomal storage disease; Mucopolysaccharidosis type II

Indexed keywords

ARTICLE; CHILD; FALSE NEGATIVE RESULT; HEALTH CARE SURVEY; HUMAN; HUNTER SYNDROME; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; PROCESS DEVELOPMENT; PROSPECTIVE STUDY; SCHOOL CHILD; SCREENING;

DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; MALE; MUCOPOLYSACCHARIDOSIS II; REGISTRIES; SYMPTOM ASSESSMENT;

EID: 84880170659     PISSN: 03406199     EISSN: 14321076     Source Type: Journal    
DOI: 10.1007/s00431-013-1967-x     Document Type: Article

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