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Paper Details

Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia.
Am J Hum Genet
179
2003
AD SCA, AD SCAs, AT08, CTG, PKC gamma, PRKCG, Purkinje cells, SCA, SCAs, amino acid, ataxia, ataxin 1, calbindin, chromosome 19q13, cysteine, dominant nonepisodic cerebellar ataxia, eye-movement disturbances, hereditary ataxias, incoordination of gait and limbs, loci, neurodegenerative conditions, neuronal, neuronal cell dysfunction, nucleotide, nucleotide repeat, patients, phorbol ester, polyglutamine, polyglutamine-related neurodegeneration, protein kinase C gamma, serine, serine/threonine kinases, spinocerebellar ataxia, threonine, trinucleotide, zinc
Author NameAffiliation
Dong-Hui ChenUniversity of Washington School of Medicine
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