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La deleción del ADN asociada con la neuropatía hereditaria con la responsabilidad de las parálisis por presión

P F Chance1, M K Alderson, K A Leppig

  • 1Department of Pediatrics, University of Utah Medical Center, Salt Lake City 84132.

Cell
|January 15, 1993
PubMed
Resumen

La neuropatía hereditaria con propensión a las parálisis por presión (HNPP) está relacionada con una deleción del cromosoma 17p11.2. Esta supresión, que afecta al gen PMP-22, sugiere que su subexpresión causa HNPP, un trastorno nervioso periférico.

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