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Delineation of the KIAA2022 mutation phenotype: Two patients with X‐linked intellectual disability and distinctive features
Authors:Yukiko Kuroda  Ikuko Ohashi  Takuya Naruto  Kazumi Ida  Yumi Enomoto  Toshiyuki Saito  Jun‐ichi Nagai  Takahito Wada  Kenji Kurosawa
Affiliation:1. Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan;2. Department of Clinical Laboratory, Kanagawa Children's Medical Center, Yokohama, Japan;3. Division of Pediatric Neurology, Kanagawa Children's Medical Center, Yokohama, Japan
Abstract:
Keywords:KIAA2022  X‐linked intellectual disability  targeted sequencing  next‐generation sequencing
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