Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type I
about
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patientsDevelopment of a diagnostic DNA chip to screen for 30 autosomal recessive disorders in the Hutterite populationCone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments.
P2860
Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type I
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年學術文章
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2012年學術文章
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2012年學術文章
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name
Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type I
@ast
Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type I
@en
type
label
Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type I
@ast
Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type I
@en
prefLabel
Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type I
@ast
Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type I
@en
P2093
P2860
P1433
P1476
Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type I
@en
P2093
Chaeli Lenger
Ian MacDonald
Ordan Lehmann
Richard Smith
William J Kimberling
P2860
P304
P577
2012-05-31T00:00:00Z