A Japanese case of oculopharyngeal muscular dystrophy (OPMD) with PABPN1 c.35G > C; p.Gly12Ala point mutation

por Nishii, Yo-suke, Noto, Yu-ichi, Yasuda, Rei, Kitaoji, Takamasa, Ashida, Shinji, Tanaka, Eijirou, Minami, Narihiro, Nishino, Ichizo, Mizuno, Toshiki
Publicado 2021