(Q57784505)

English

The Phenotype of Severe Early Childhood Onset Retinal Dystrophy (SECORD) from Mutation ofRPE65and Differentiation from Leber Congenital Amaurosis

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title

The Phenotype of Severe Early Childhood Onset Retinal Dystrophy (SECORD) from Mutation ofRPE65and Differentiation from Leber Congenital Amaurosis (English)

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main subject

Leber congenital amaurosis

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1 reference

Edwin M. Stone

5

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author name string

Richard G. Weleber

series ordinal

1

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Michel Michaelides

series ordinal

2

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Karmen M. Trzupek

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3

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Niamh B. Stover

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4

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language of work or name

English

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publication date

5 January 2011

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published in

Investigative Ophthalmology Visual Science

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volume

52

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issue

1

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page(s)

292

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Identifiers

DOI

10.1167/IOVS.10-6106

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PubMed publication ID

20811047

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(Q57784505)

The Phenotype of Severe Early Childhood Onset Retinal Dystrophy (SECORD) from Mutation ofRPE65and Differentiation from Leber Congenital Amaurosis

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