Stringer, R. N., Jurkovicova-Tarabova, B., Huang, S., Haji-Ghassemi, O., Idoux, R., Liashenko, A., . . . Weiss, N. (2020). A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Ca(v)3.2 T-type channel activity. Mol Brain.
Styl ChicagoStringer, Robin N., et al. "A Rare CACNA1H Variant Associated With Amyotrophic Lateral Sclerosis Causes Complete Loss of Ca(v)3.2 T-type Channel Activity." Mol Brain 2020.
Citace podle MLAStringer, Robin N., et al. "A Rare CACNA1H Variant Associated With Amyotrophic Lateral Sclerosis Causes Complete Loss of Ca(v)3.2 T-type Channel Activity." Mol Brain 2020.
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