New Articles From Orphanet Journal of Rare Diseases

Orphanet Journal of Rare Diseases

The following new articles have just been published in Orphanet Journal of Rare Diseases RESEARCH Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss Nobuko Yamamoto, Hideki Mutai, Kazunori Namba, Noriko Morita, Shin Masuda, Yasuyuki Nishi, Atsuko Nakano, Sawako Masuda, Masato Fujioka, Kimitaka Kaga, Kaoru Ogawa and Tatsuo Matsunaga Orphanet Journal of Rare Diseases 2017, 12:157 | Published on: 25 September 2017 Full Text | PDF

For further information or enquiries please contact the Support Team at:info@biomedcentral.com BioMed Central Ltd 236 Gray's Inn Road, London, WC1X 8HB, United Kingdom Privacy Policy