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http://purl.uniprot.org/citations/12124997http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/12124997http://www.w3.org/2000/01/rdf-schema#comment"The Wiskott-Aldrich Syndrome (WAS) is an X-linked recessive immunodeficiency caused by mutation in the gene encoding WAS protein (WASP). The disease is characterized by eczema, thrombocytopenia and severe immunodeificency and is associated with extensive clinical heterogeneity. Mutation studies indicated that the mutated genotypes are also highly variable. In this study, we performed PCR-direct sequencing analysis of the WAS gene in six unrelated Chinese families. Five novel mutations identified, included two nonsense mutations (506C-->T, 1388-->T), a small insertion (685-686insCGCA) and two single-base deletions (384delT, 984delC). All of the mutations are predicted to lead to premature translational termination of WASP."xsd:string
http://purl.uniprot.org/citations/12124997http://purl.org/dc/terms/identifier"doi:10.1002/humu.9048"xsd:string
http://purl.uniprot.org/citations/12124997http://purl.uniprot.org/core/author"Yang X."xsd:string
http://purl.uniprot.org/citations/12124997http://purl.uniprot.org/core/author"Chan K.W."xsd:string
http://purl.uniprot.org/citations/12124997http://purl.uniprot.org/core/author"Chung B.H."xsd:string
http://purl.uniprot.org/citations/12124997http://purl.uniprot.org/core/author"Lau Y.L."xsd:string
http://purl.uniprot.org/citations/12124997http://purl.uniprot.org/core/author"Lee T.L."xsd:string
http://purl.uniprot.org/citations/12124997http://purl.uniprot.org/core/date"2002"xsd:gYear
http://purl.uniprot.org/citations/12124997http://purl.uniprot.org/core/name"Hum Mutat"xsd:string
http://purl.uniprot.org/citations/12124997http://purl.uniprot.org/core/pages"151-152"xsd:string
http://purl.uniprot.org/citations/12124997http://purl.uniprot.org/core/title"Identification of five novel WASP mutations in Chinese families with Wiskott-Aldrich syndrome."xsd:string
http://purl.uniprot.org/citations/12124997http://purl.uniprot.org/core/volume"20"xsd:string
http://purl.uniprot.org/citations/12124997http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/12124997
http://purl.uniprot.org/citations/12124997http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/12124997
http://purl.uniprot.org/uniprot/#_A0A8V8TM35-mappedCitation-12124997http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12124997
http://purl.uniprot.org/uniprot/#_P42768-mappedCitation-12124997http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12124997
http://purl.uniprot.org/uniprot/#_Q2PAL5-mappedCitation-12124997http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12124997
http://purl.uniprot.org/uniprot/P42768http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/12124997
http://purl.uniprot.org/uniprot/Q2PAL5http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/12124997
http://purl.uniprot.org/uniprot/A0A8V8TM35http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/12124997