| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8754777 | Auris Nasus Larynx | 2018 | 7 Pages |
Abstract
Japanese PCD patients have novel mutations in cilia-related genes. This targeted NGS panel can identify disease-causing mutations in patients with PCD.
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Authors
Kazuhiko Takeuchi, Masako Kitano, Hiroko Kiyotoshi, Koji Ikegami, Satoru Ogawa, Makoto Ikejiri, Mizuho Nagao, Takao Fujisawa, Kaname Nakatani,