Rapid detection of duplication/deletion of the PMP22 gene in patients with Charcot-Marie-Tooth disease Type 1A and hereditary neuropathy with liability to pressure palsy by real-time quantitative PCR using SYBR Green I dye.

Gelijkaardige items

• PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies
  door: van Paassen, Barbara W, et al.
  Gepubliceerd in: (2014)
• Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A.
  door: Chapon, F, et al.
  Gepubliceerd in: (1996)
• Rapid genetic screening of Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies patients★
  door: Li, Xiaobo, et al.
  Gepubliceerd in: (2012)
• A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy
  door: Hong, Young Bin, et al.
  Gepubliceerd in: (2016)
• Effectiveness of Real-Time Quantitative PCR Compare to Repeat PCR for the Diagnosis of Charcot-Marie-Tooth Type 1A and Hereditary Neuropathy with Liability to Pressure Palsies
  door: Choi, Jong Rak, et al.
  Gepubliceerd in: (2005)