A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family.
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Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan.A nonsense mutation in S-antigen (p.Glu306*) causes Oguchi disease.Lessons from photoreceptors: turning off g-protein signaling in living cells.Schizophrenia and cortical blindness: protective effects and implications for languageA novel missense mutation of the GRK1 gene in Oguchi diseaseThe molecular basis of retinal dystrophies in pakistan.
P2860
A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 05 September 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family.
@en
A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family.
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A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family.
@en
A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family.
@nl
prefLabel
A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family.
@en
A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family.
@nl
P2093
P2860
P1433
P1476
A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family
@en
P2093
Anneke I den Hollander
Frans P M Cremers
Maleeha Azam
Muhammad Ajmal
Muhammad Imran Khan
Nadeem Qureshi
Raheel Qamar
Rob W J Collin
P2860
P304
P577
2009-09-05T00:00:00Z