Records 1 - 4
| Genetic association of MYH genes with hereditary hearing loss in Korea.
Gene 2016 Jul .
Kim Sang-Joo, Lee Seokwon, Park Hong-Joon, Kang Tae-Hun, Sagong Borum, Baek Jeong-In, Oh Se-Kyung, Choi Jae Young, Lee Kyu-Yup, Kim Un-Kyu
| Late onset and high-frequency dominant hearing loss in a family with MYH9 disorder.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2016 Mar .
Wasano Koichiro, Matsunaga Tatsuo, Ogawa Kaoru, Kunishima Shin
| Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease.
Ear and hearing 2015 Jul .
Verver Eva J J, Topsakal Vedat, Kunst Henricus P M, Huygen Patrick L M, Heller Paula G, Pujol-Moix Nuria, Savoia Anna, Benazzo Marco, Fierro Tiziana, Grolman Wilko, Gresele Paolo, Pecci Alessand
| Mutations in MYH9 exons 1, 16, 26, and 30 are infrequently found in Japanese patients with nonsyndromic deafness.
Genetic testing and molecular biomarkers 2009 Oct 13 (5): 705-7.
Kunishima Shinji, Matsunaga Tatsuo, Ito Yoshimi, Saito Hidehi