Craig L. Bennett
Division of Genetics and Developmental Medicine
Department of Pediatrics
University of Washington
and Children's Hospital and Regional Medical Center
USA
Name/email consistency: medium
- Prevalence of ALDH7A1 mutations in 18 North American pyridoxine-dependent seizure (PDS) patients. Bennett, C.L., Chen, Y., Hahn, S., Glass, I.A., Gospe, S.M. Epilepsia (2009)
- Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizures. Bennett, C.L., Huynh, H.M., Chance, P.F., Glass, I.A., Gospe, S.M. Neurogenetics (2005)
- Joubert syndrome: a haplotype segregation strategy and exclusion of the zinc finger protein of cerebellum 1 (ZIC1) gene. Bennett, C.L., Parisi, M.A., Eckert, M.L., Huynh, H.M., Chance, P.F., Glass, I.A. Am. J. Med. Genet. A (2004)
- SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve. Bennett, C.L., Shirk, A.J., Huynh, H.M., Street, V.A., Nelis, E., Van Maldergem, L., De Jonghe, P., Jordanova, A., Guergueltcheva, V., Tournev, I., Van Den Bergh, P., Seeman, P., Mazanec, R., Prochazka, T., Kremensky, I., Haberlova, J., Weiss, M.D., Timmerman, V., Bird, T.D., Chance, P.F. Ann. Neurol. (2004)
