Profound infantile neuroretinal dysfunction in a heterozygote for the CLN3 genetic defect.
about
Using Stem Cells to Model Diseases of the Outer RetinaJuvenile neuronal ceroid lipofuscinosis (JNCL) and the eye.Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses.Using Patient-Specific Induced Pluripotent Stem Cells and Wild-Type Mice to Develop a Gene Augmentation-Based Strategy to Treat CLN3-Associated Retinal Degeneration
P2860
Profound infantile neuroretinal dysfunction in a heterozygote for the CLN3 genetic defect.
description
2004 nî lūn-bûn
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2004年の論文
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2004年学术文章
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2004年学术文章
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name
Profound infantile neuroretina ...... e for the CLN3 genetic defect.
@en
Profound infantile neuroretina ...... e for the CLN3 genetic defect.
@nl
type
label
Profound infantile neuroretina ...... e for the CLN3 genetic defect.
@en
Profound infantile neuroretina ...... e for the CLN3 genetic defect.
@nl
prefLabel
Profound infantile neuroretina ...... e for the CLN3 genetic defect.
@en
Profound infantile neuroretina ...... e for the CLN3 genetic defect.
@nl
P2093
P2860
P1476
Profound infantile neuroretina ...... e for the CLN3 genetic defect.
@en
P2093
Charles Glasier
Emily de los Reyes
Michael Brodsky
Paul Phillips
Paul Richard Dyken
Robert E Mrak
Stephen Bates
P2860
P356
10.1177/08830738040190010703
P577
2004-01-01T00:00:00Z