Genomic backgrounds of Japanese patients with undiagnosed neurodevelopmental disorders

Recently, many genes related to neurodevelopmental disorders have been identified by high-throughput genomic analysis; however, a comprehensive understanding of the mechanism underlying neurodevelopmental disorders remains to be established. To further understand these underlying mechanisms, we perf...

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Veröffentlicht in:	Brain & development (Tokyo. 1979) 2019-10, Vol.41 (9), p.776-782
Hauptverfasser:	Yamamoto, Toshiyuki, Imaizumi, Taichi, Yamamoto-Shimojima, Keiko, Lu, Yongping, Yanagishita, Tomoe, Shimada, Shino, Chong, Pin Fee, Kira, Ryutaro, Ueda, Riyo, Ishiyama, Akihiko, Takeshita, Eri, Momosaki, Ken, Ozasa, Shiro, Akiyama, Tomoyuki, Kobayashi, Katsuhiro, Oomatsu, Hiroo, Kitahara, Hikaru, Yamaguchi, Tokito, Imai, Katsumi, Kurahashi, Hirokazu, Okumura, Akihisa, Oguni, Hirokazu, Seto, Toshiyuki, Okamoto, Nobuhiko
Format:	Artikel
Sprache:	eng
Schlagworte:	Asian Continental Ancestry Group - genetics Child, Preschool DNA Copy Number Variations Dysmorphism Female Genetic Predisposition to Disease Genomic copy number variations Humans Japan Male Neurodevelopmental Disorders - genetics Polymorphism, Single Nucleotide Single nucleotide variants X-linked recessive
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