Autosomal dominant optic atrophy with OPA1 gene mutations accompanied by auditory neuropathy and other systemic complications in a Japanese cohort.

Published in:

Molecular Vision, 2019, v. 25, p. 559

By:

• Akiko Maeda-Katahira;
• Natsuko Nakamura;
• Takaaki Hayashi;
• Satoshi Katagiri;
• Satoko Shimizu;
• Hisao Ohde;
• Tatsuo Matsunaga;
• Kimitaka Kaga;
• Tadashi Nakano;
• Shuhei Kameya;
• Tomokazu Matsuura;
• Kaoru Fujinami;
• Takeshi Iwata;
• Kazushige Tsunoda

Publication type:

Article