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searching for EFHC1 2 found (10 total)

alternate case: eFHC1

Genetics of synesthesia (1,145 words) [view diff] exact match in snippet view article find links to article

the development of the cerebral cortex (TBR1), dyslexia, and apoptosis (EFHC1), the last of which could be potentially related to the retention of the

R-type calcium channel (1,325 words) [view diff] exact match in snippet view article find links to article

Osawa M, Kaneko S, Oguni H, Mori Y, Yamakawa K (August 2004). "Mutations in EFHC1 cause juvenile myoclonic epilepsy". Nature Genetics. 36 (8): 842–9. doi:10