CXorf6 is a causative gene for hypospadias

Maki Fukami, Yuka Wada, Kanako Miyabayashi, Ichizo Nishino, Tomonobu Hasegawa, Giovanna Camerino, Christine Kretz, Anna Buj-Bello, Jocelyn Laporte, Gen Yamada, Ken Ichirou Morohashi, Tsutomu Ogata

研究成果: Contribution to journalArticle

100 引用 (Scopus)

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46,XY disorders of sex development (DSD) refer to a wide range of abnormal genitalia, including hypospadias, which affects ∼0.5% of male newborns. We identified three different nonsense mutations of CXorf6 in individuals with hypospadias and found that its mouse homolog was specifically expressed in fetal Sertoli and Leydig cells around the critical period for sex development. These data imply that CXorf6 is a causative gene for hypospadias.

元の言語英語
ページ(範囲)1369-1371
ページ数3
ジャーナルNature genetics
38
発行部数12
DOI
出版物ステータス出版済み - 12 5 2006

All Science Journal Classification (ASJC) codes

  • Genetics

フィンガープリント CXorf6 is a causative gene for hypospadias' の研究トピックを掘り下げます。これらはともに一意のフィンガープリントを構成します。

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    Fukami, M., Wada, Y., Miyabayashi, K., Nishino, I., Hasegawa, T., Camerino, G., Kretz, C., Buj-Bello, A., Laporte, J., Yamada, G., Morohashi, K. I., & Ogata, T. (2006). CXorf6 is a causative gene for hypospadias. Nature genetics, 38(12), 1369-1371. https://doi.org/10.1038/ng1900