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No mutations in the coding region of the PRKCG gene in three families with retinitis pigmentosa linked to the RP11 locus on chromosome 19q.
PMID: 10441600 [PubMed - indexed for MEDLINE]
PMCID: PMC1378000
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Cited by 1 PubMed Central article
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Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia.
Chen DH, Brkanac Z, Verlinde CL, Tan XJ, Bylenok L, Nochlin D, Matsushita M, Lipe H, Wolff J, Fernandez M, et al.
Am J Hum Genet. 2003 Apr; 72(4):839-49. Epub 2003 Mar 17.
[Am J Hum Genet. 2003]