Počet záznamů: 1
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. Roč. 13, č. 1 (2019), s. 153-161. ISSN 1933-6950. E-ISSN 1933-6969
Obor OECD: Biochemistry and molecular biology
Impakt faktor: 2.311, rok: 2019
Způsob publikování: Open access
https://www.tandfonline.com/doi/full/10.1080/19336950.2019.1614415
http://hdl.handle.net/11104/0296979
Počet záznamů: 1