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A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
Published on: June 15, 2011
Extending the critical regions for mutations in the non-coding gene RNU4ATAC in another patient with Roifman Syndrome
Ariane Hallermayr1, Janine Graf1, Udo Koehler1
1MGZ - Medical Genetics Center Munich Germany.
Abstract:
Compound heterozygosity of a previously described pathogenic variant and a second novel nucleotide substitution (NR_023343.1:n.116A>C) affecting a highly conserved nucleotide in the noncoding RNU4ATAC gene could be identified in a patient with overlapping features of Roifman Syndrome. These data extend the spectrum of pathogenic variants in RNU4ATAC.
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