Sequence variations of GRM6 in patients with high myopia.
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Trio-based exome sequencing arrests de novo mutations in early-onset high myopiaWhole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindnessInterpretation of mRNA splicing mutations in genetic disease: review of the literature and guidelines for information-theoretical analysis.ON pathway mutations increase susceptibility to form-deprivation myopia.Mutations in GRM6 identified in consanguineous Pakistani families with congenital stationary night blindness.Novel TRPM1 mutations in two Chinese families with early-onset high myopia, with or without complete congenital stationary night blindness.The Transduction Cascade in Retinal ON-Bipolar Cells: Signal Processing and Disease."mGlu Receptors in the Retina" - WIREs Membrane Transport and Signaling.Association of ZNF644, GRM6, and CTNND2 genes with high myopia in the Han Chinese population: Jiangsu Eye Study.
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Sequence variations of GRM6 in patients with high myopia.
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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 19 October 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Sequence variations of GRM6 in patients with high myopia.
@en
Sequence variations of GRM6 in patients with high myopia.
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label
Sequence variations of GRM6 in patients with high myopia.
@en
Sequence variations of GRM6 in patients with high myopia.
@nl
prefLabel
Sequence variations of GRM6 in patients with high myopia.
@en
Sequence variations of GRM6 in patients with high myopia.
@nl
P2093
P2860
P1433
P1476
Sequence variations of GRM6 in patients with high myopia
@en
P2093
Panfeng Wang
Qingjiong Zhang
Shiqiang Li
Xiangming Guo
Xueshan Xiao
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P304
P577
2009-10-19T00:00:00Z