ABCA4 midigenes reveal the full splice spectrum of all reported noncanonical splice site variants in Stargardt disease.
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RNA Biology in Retinal Development and Disease.Special Issue Introduction: Inherited Retinal Disease: Novel Candidate Genes, Genotype-Phenotype Correlations, and Inheritance Models.Identification and Rescue of Splice Defects Caused by Two Neighboring Deep-Intronic ABCA4 Mutations Underlying Stargardt Disease.Correlating the Expression and Functional Activity of ABCA4 Disease Variants With the Phenotype of Patients With Stargardt Disease.Expanding the Mutation Spectrum in : Sixty Novel Disease Causing Variants and Their Associated Phenotype in a Large French Stargardt Cohort
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ABCA4 midigenes reveal the full splice spectrum of all reported noncanonical splice site variants in Stargardt disease.
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ABCA4 midigenes reveal the ful ...... variants in Stargardt disease.
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ABCA4 midigenes reveal the ful ...... variants in Stargardt disease.
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ABCA4 midigenes reveal the ful ...... variants in Stargardt disease.
@en
ABCA4 midigenes reveal the ful ...... variants in Stargardt disease.
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ABCA4 midigenes reveal the ful ...... variants in Stargardt disease.
@en
ABCA4 midigenes reveal the ful ...... variants in Stargardt disease.
@nl
P2093
P2860
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ABCA4 midigenes reveal the ful ...... variants in Stargardt disease
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P2093
Alejandro Garanto
Dorien Lugtenberg
Duaa Elmelik
Frans P M Cremers
L Ingeborgh van den Born
Mubeen Khan
Raheel Qamar
Rob W J Collin
Stéphanie S Cornelis
Valerie Richelle
P2860
P304
P356
10.1101/GR.226621.117
P577
2017-11-21T00:00:00Z