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Taylor and Francis Group, Channels, 1(13), p. 153-161, 2019

DOI: 10.1080/19336950.2019.1614415

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Compound heterozygous CACNA1H mutations associated with severe congenital amyotrophy

Journal article published in 2019 by Melissa T. Carter ORCID, Andriy Tomin ORCID, Norbert Weiss ORCID, Hugh J. McMillan ORCID
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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