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

por Maeda-Katahira, Akiko, Nakamura, Natsuko, Hayashi, Takaaki, Katagiri, Satoshi, Shimizu, Satoko, Ohde, Hisao, Matsunaga, Tatsuo, Kaga, Kimitaka, Nakano, Tadashi, Kameya, Shuhei, Matsuura, Tomokazu, Fujinami, Kaoru, Iwata, Takeshi, Tsunoda, Kazushige
Publicado 2019