A Japanese Patient with Hereditary Myopathy with Early Respiratory Failure Due to the p.P31732L Mutation of Titin.

Autor: Yasuteru Sano, Satoko Ota, Mariko Oishi, Masaya Honda, Masatoshi Omoto, Motoharu Kawai, Mariko Okubo, Ichizo Nishino, Takashi Kanda
Zdroj: Internal Medicine; 2022, Vol. 61 Issue 10, p1587-1592, 6p
Databáze: Complementary Index