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Familial focal segmental glomerulosclerosis with PLCE1 mutation in siblings.

Masaki ShimizuHitoshi IrabuHisashi KanedaKazuhide OhtaKandai Nozu
Published in: Pediatrics international : official journal of the Japan Pediatric Society (2020)
Keyphrases
  • early onset
  • intellectual disability
  • autism spectrum disorder