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RP23 gene

Known as: RETINITIS PIGMENTOSA 23, RP23 
National Institutes of Health

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2 relations
Decreased night visionMAPRE2 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2012
Highly Cited
2012
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23).
X-linked retinitis pigmentosa (XLRP) is genetically heterogeneous with two causative genes identified, RPGR and RP2. We… 
Highly Cited
2007
Highly Cited
2007
Defining the expression pattern of the LGI1 gene in BAC transgenic mice
The LGI1 gene has been implicated in the development of epilepsy and the invasion phenotype of glial cells. Controversy over the… 
2000
2000
Evidence for a new locus for X-linked retinitis pigmentosa (RP23).
PURPOSE X-linked retinitis pigmentosa (XLRP) is a degenerative disease of the retina characterized in the early stages of disease… 
1983
1983
Establishment of lymphoblastoid cell lines from Marek's disease primary tumors.
Seven lymphoblastoid cell lines were developed from 15 Marek's disease primary lymphomas treated to remove adherent cells (46.7… 
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