Identification of a novel mutation in the humanPDE6Agene in autosomal recessive retinitis pigmentosa: homology with thenmf28/nmf28mice model
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Mutations in MAPKBP1 Cause Juvenile or Late-Onset Cilia-Independent NephronophthisisInfliximab reduces Zaprinast-induced retinal degeneration in cultures of porcine retina.Splice-site mutations identified in PDE6A responsible for retinitis pigmentosa in consanguineous Pakistani families.Genetic variation in phosphodiesterase (PDE) 7B in chronic lymphocytic leukemia: overview of genetic variants of cyclic nucleotide PDEs in human disease.Efficacy of PARP inhibition in Pde6a mutant mouse models for retinitis pigmentosa depends on the quality and composition of individual human mutations.Novel PDE6A mutation in an Emirati patient with retinitis pigmentosa.
P2860
Identification of a novel mutation in the humanPDE6Agene in autosomal recessive retinitis pigmentosa: homology with thenmf28/nmf28mice model
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article
@en
im November 2010 veröffentlichter wissenschaftlicher Artikel
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wetenschappelijk artikel
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наукова стаття, опублікована в жовтні 2010
@uk
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Identification of a novel muta ...... with thenmf28/nmf28mice model
@en
Identification of a novel muta ...... with thenmf28/nmf28mice model
@nl
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Identification of a novel muta ...... with thenmf28/nmf28mice model
@en
Identification of a novel muta ...... with thenmf28/nmf28mice model
@nl
prefLabel
Identification of a novel muta ...... with thenmf28/nmf28mice model
@en
Identification of a novel muta ...... with thenmf28/nmf28mice model
@nl
P2860
P50
P1433
P1476
Identification of a novel muta ...... ith the nmf28/nmf28 mice model
@en
P2093
M J Blanco
M Sanchez-Salorio
P2860
P304
P356
10.1111/J.1399-0004.2010.01487.X
P577
2010-11-01T00:00:00Z