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Compound heterozygous CACNA1H mutations associated with severe congenital amyotrophy
- 1.CARTER, M. T., MCMILLAN, H. J., TOMIN, Andriy, WEISS, Norbert. Compound heterozygous CACNA1H mutations associated with severe congenital amyotrophy. Channels. 2019, 13(1), 153-161. ISSN 1933-6950. E-ISSN 1933-6969. Available: doi: 10.1080/19336950.2019.1614415.
Number of the records: 1