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0505495 - ÚOCHB 2020 RIV US eng J - Journal Article
Carter, M. T. - McMillan, H. J. - Tomin, Andriy - Weiss, Norbert
Compound heterozygous CACNA1H mutations associated with severe congenital amyotrophy.
Channels. Roč. 13, č. 1 (2019), s. 153-161. ISSN 1933-6950. E-ISSN 1933-6969
Institutional support: RVO:61388963
Keywords : congenital amyotrophy * CACNA1H * mutations * calcium channel * Ca(v)3.2 channel * T-type channel
OECD category: Biochemistry and molecular biology
Impact factor: 2.311, year: 2019
Method of publishing: Open access
https://www.tandfonline.com/doi/full/10.1080/19336950.2019.1614415
Permanent Link: http://hdl.handle.net/11104/0296979