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 |
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Zdroj: | Internal Medicine; 2022, Vol. 61 Issue 10, p1587-1592, 6p |
Databáze: | Complementary Index |
Externí odkaz: |