PubMed:22669887 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/22669887","sourcedb":"PubMed","sourceid":"22669887","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/22669887","text":"Purine nucleoside phosphorylase deficiency with a novel PNP gene mutation: a first case report from India.\nThe authors report a case of purine nucleoside phosphorylase (PNP) deficiency for the first time from India. The case presented with recurrent severe infections, developmental delays, seizures and progressive neurological deterioration. The diagnosis of primary immunodeficiency disorder was delayed in spite of recurrent infection due to predominant neurological symptoms. Sequencing of the PNP gene revealed a novel mutation resulting in a premature stop 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