Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia
- DOI
- 10.1016/s0887-8994(01)00371-x
- Published
- 2002-01
- Container
- Pediatric Neurology
- Publisher
- Elsevier BV
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/s0887-8994-01-00371-x,
title = {Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia},
author = {Takahito Wada and Norio Kobayashi and Yoshio Takahashi and Tomoko Aoki and Takako Watanabe and Shinji Saitoh},
year = {2002},
journal = {Pediatric Neurology},
doi = {10.1016/s0887-8994(01)00371-x},
url = {https://doi.org/10.1016/s0887-8994(01)00371-x}
}RIS
TY - JOUR TI - Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia AU - Takahito Wada AU - Norio Kobayashi AU - Yoshio Takahashi AU - Tomoko Aoki AU - Takako Watanabe AU - Shinji Saitoh PY - 2002 JO - Pediatric Neurology DO - 10.1016/s0887-8994(01)00371-x UR - https://doi.org/10.1016/s0887-8994(01)00371-x ER -
APA
Wada, T., Kobayashi, N., Takahashi, Y., Aoki, T., Watanabe, T., & Saitoh, S. (2002). Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia. Pediatric Neurology. https://doi.org/10.1016/s0887-8994(01)00371-x
Source records
- crossref · retrieved 2026-11-10T15:04:34.527Z