Human Genome Epidemiology Literature Finder
|
Records 1 - 7 (of 7 Records) |
| Query Trace: Vertigo and SLC26A4[original query] |
|---|
| Clinical characteristics and genotype-phenotype correlation of hearing loss patients with SLC26A4 mutations. Acta oto-laryngologica 2007 Dec 127 (12): 1292-7. Suzuki Hiroaki, Oshima Aki, Tsukamoto Koji, Abe Satoko, Kumakawa Kozo, Nagai Kyoko, Satoh Hitoshi, Kanda Yukihiko, Iwasaki Satoshi, Usami Shin-ic |
| Mutation spectrum and genotype-phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort study. Journal of human genetics 2014 May 59 (5): 262-8. Miyagawa Maiko, Nishio Shin-Ya, Usami Shin-Ichi, |
| Discrepancies between video head impulse and caloric tests in patients with enlarged vestibular aqueduct. The Laryngoscope 2016 Jul . Jung Jinsei, Suh Michelle J, Kim Sung Hu |
| Vestibular function is associated with residual low-frequency hearing loss in patients with bi-allelic mutations in the SLC26A4 gene. Hearing research 2016 Feb . Jung Jinsei, Seo Young Wook, Choi Jae Young, Kim Sung Hu |
| Excess of Rare Missense Variants in Hearing Loss Genes in Sporadic Meniere Disease. Frontiers in genetics 2019 10 76. Gallego-Martinez Alvaro, Requena Teresa, Roman-Naranjo Pablo, Lopez-Escamez Jose |
| Genetic Susceptibility Study of Chinese Sudden Sensorineural Hearing Loss Patients with Vertigo. Current medical science 2021 Aug 41 (4): 673-679. Gao Yun, Wang Hong-Yang, Guan Jing, Lan Lan, Zhao Cui, Xie Lin-Yi, Wang Da-Yong, Wang Qiu- |
| Clinical and genetic analysis of children with hearing loss and bilateral enlarged vestibular aqueducts. International journal of pediatric otorhinolaryngology 2021 11 152 110975. Nakano Atsuko, Arimoto Yukiko, Mutai Hideki, Nara Kiyomitsu, Inoue Satomi, Matsunaga Tats |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 04, 2023
- Content source: