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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
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A novel homozygous mutation in the WNK1/HSN2 gene causing hereditary sensory neuropathy type 2

Anna Potulska-Chromik1, Dagmara Kabzińska, Marta Lipowska

  • 1Department of Neurology, Medical University of Warsaw, Poland.

Acta Biochimica Polonica
|August 23, 2012
PubMed

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