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5
导致人视网膜色素变性的RPGR基因突变.pdf
导致人视网膜色素变性的RPGR基因突变突变,引起,造成,变性导致,基因突变,视网膜变性,视网膜脱落
2篇相似文档
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8
Mutational analysis of RPGR and RP2 genes in Japanese patients....pdf
Mutational analysis of RPGR and RP2 genes in Japanese patients…
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2
A presumed missense mutation of RPGR causes abnormal RNA splicing with exon skipping.pdf
A presumed missense mutation of RPGR causes abnormal RNA splicing with exon skipping
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5
RPGR-containing protein complexes in syndromic and non-syndromic retinal degeneration due to ciliary dysfunction.pdf
RPGR-containing protein complexes in syndromic and non-syndromic retinal degeneration due to ciliary dysfunction
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6
sequence variation within the lt;em gt;rpgr lt;em gt; gene evidence for a founder complex allele.pdf
sequence variation within the
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5
X-Linked Cone-Rod Dystrophy (Locus COD1) Identification of Mutations in RPGR Exon ORF15.pdf
X-Linked Cone-Rod Dystrophy (Locus COD1) Identification of Mutations in RPGR Exon ORF15
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3
A Novel RPGR Exon ORF15 Mutation in a Family With X-linked Retinitis Pigmentosa and Coats'-like Exudative Vasculopathy.pdf
A Novel RPGR Exon ORF15 Mutation in a Family With X-linked Retinitis Pigmentosa and Coats’-like Exudative Vasculopathy
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3
Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15.pdf
Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15
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7
Rates of Decline in Regions of the Visual Field Defined by Frequency-Domain Optical Coherence Tomography in Patients with RPGR-Mediated X-Linked Retinitis Pigmentosa.pdf
Rates of Decline in Regions of the Visual Field Defined by Frequency-Domain Optical Coherence Tomography in Patients with RPGR-Mediated X-Linked Retinitis Pigmentosa
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5
identification of a 5 splice site mutation in the lt;em gt;rpgr lt;em gt; gene in a family with x-linked retinitis pigmentosa (rp3).pdf
identification of a 5′ splice site mutation in the
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