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http://purl.uniprot.org/citations/28778786http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/28778786http://www.w3.org/2000/01/rdf-schema#comment"CDK5RAP2 gene encodes a centrosomal protein, highly expressed in fetal brain and essentially indispensable for its normal development, as biallelic mutations in it lead to primary microcephaly (MCPH). Despite being known as MCPH linked gene for more than a decade, the phenotypic spectrum of CDK5RAP2 mutations is still under explored as only eleven families have been reported worldwide. Here, we analyzed a consanguineous Pakistani MCPH family, characterized by moderate to severe intellectual disability, speech impairment, moderately short stature and sparse eyebrows. Whole exome sequencing of the proband identified a 2bp duplication in exon 34 of CDK5RAP2 that causes frame-shift, leading to a premature stop codon. The resultant transcript is resistant to nonsense mediated decay, suggesting that the mutation leads to a truncated protein lacking C-terminal domains; CDK5R1, and Cnn motif 2 (CM2), required for its localization to centrosome and Golgi Apparatus. Clinical variability observed in the family highlights the importance of further detailed clinical description of patients with CDK5RAP2 mutations."xsd:string
http://purl.uniprot.org/citations/28778786http://purl.org/dc/terms/identifier"doi:10.1016/j.ejmg.2017.07.017"xsd:string
http://purl.uniprot.org/citations/28778786http://purl.uniprot.org/core/author"Tommerup N."xsd:string
http://purl.uniprot.org/citations/28778786http://purl.uniprot.org/core/author"Hansen L."xsd:string
http://purl.uniprot.org/citations/28778786http://purl.uniprot.org/core/author"Farooq M."xsd:string
http://purl.uniprot.org/citations/28778786http://purl.uniprot.org/core/author"Kjaer K.W."xsd:string
http://purl.uniprot.org/citations/28778786http://purl.uniprot.org/core/author"Larsen L.A."xsd:string
http://purl.uniprot.org/citations/28778786http://purl.uniprot.org/core/author"Fatima A."xsd:string
http://purl.uniprot.org/citations/28778786http://purl.uniprot.org/core/author"Abdullah U."xsd:string
http://purl.uniprot.org/citations/28778786http://purl.uniprot.org/core/author"Mang Y."xsd:string
http://purl.uniprot.org/citations/28778786http://purl.uniprot.org/core/author"Mahmood Baig S."xsd:string
http://purl.uniprot.org/citations/28778786http://purl.uniprot.org/core/author"Faryal S."xsd:string
http://purl.uniprot.org/citations/28778786http://purl.uniprot.org/core/author"Marriam Bakhtiar S."xsd:string
http://purl.uniprot.org/citations/28778786http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/28778786http://purl.uniprot.org/core/name"Eur J Med Genet"xsd:string
http://purl.uniprot.org/citations/28778786http://purl.uniprot.org/core/pages"627-630"xsd:string
http://purl.uniprot.org/citations/28778786http://purl.uniprot.org/core/title"A novel mutation in CDK5RAP2 gene causes primary microcephaly with speech impairment and sparse eyebrows in a consanguineous Pakistani family."xsd:string
http://purl.uniprot.org/citations/28778786http://purl.uniprot.org/core/volume"60"xsd:string
http://purl.uniprot.org/citations/28778786http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/28778786
http://purl.uniprot.org/citations/28778786http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/28778786
http://purl.uniprot.org/uniprot/#_A0A0A0MRG9-mappedCitation-28778786http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28778786
http://purl.uniprot.org/uniprot/#_A0A0C4ZLW1-mappedCitation-28778786http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28778786
http://purl.uniprot.org/uniprot/#_B3KVI2-mappedCitation-28778786http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28778786
http://purl.uniprot.org/uniprot/#_A6H8X1-mappedCitation-28778786http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28778786