A family with both X‐linked dominant Charcot–Marie–Tooth disease and myotonic dystrophy type 1 mutations with phenotypic variations.
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| Title: | A family with both X‐linked dominant Charcot–Marie–Tooth disease and myotonic dystrophy type 1 mutations with phenotypic variations. |
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| Authors: | Mori, Chiaki1 (AUTHOR) morichia@toneyama.go.jp, Nakatani, Rie2 (AUTHOR), Nakamori, Masayuki2 (AUTHOR), Matsumura, Tsuyoshi1 (AUTHOR), Takahashi, Masanori P.2,3 (AUTHOR), Fujimura, Harutoshi1 (AUTHOR), Mochizuki, Hideki2 (AUTHOR), Sakoda, Saburo1 (AUTHOR) |
| Source: | Neurology & Clinical Neuroscience. Mar2019, Vol. 7 Issue 2, p88-90. 3p. |
| Database: | Academic Search Ultimate |
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| ISSN: | 20494173 |
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| DOI: | 10.1111/ncn3.12251 |
