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De novo 1p35.2 microdeletion including PUM1 identified in a patient with sporadic West syndrome.

Taichi ImaizumiYukiko MogamiNobuhiko OkamotoKeiko Yamamoto-ShimojimaToshiyuki Yamamoto
Published in: Congenital anomalies (2019)
Keyphrases
  • case report
  • late onset
  • amyotrophic lateral sclerosis