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Letter
Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia

Authors

  1. Correspondence to Dr Jonathan M Schott, Institute of Neurology – Dementia Research Centre, Queen Square, London WC1N 3BG, UK; j.schott{at}ucl.ac.uk
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Citation

Rohrer JD, Beck J, Plagnol V, et al
Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia

Publication history

  • First published July 31, 2013.
Online issue publication 
November 13, 2013

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