(Q42677952)

4 November 2017

title

Identification and characterization of C6orf37, a novel candidate human retinal disease gene on chromosome 6q14. (English)

1 reference

4 November 2017

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Lagali PS

1

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4 November 2017

Kakuk LE

2

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4 November 2017

Griesinger IB

3

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4 November 2017

Wong PW

4

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4 November 2017

Ayyagari R

5

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4 November 2017

language of work or name

English

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publication date

1 April 2002

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Biochemical and Biophysical Research Communications

4 November 2017

published in

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4 November 2017

volume

293

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4 November 2017

issue

1

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4 November 2017

page(s)

356-365

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North Carolina macular dystrophy is assigned to chromosome 6

4 November 2017

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Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q

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Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6q

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Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q

7 January 2021

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A major locus for autosomal recessive retinitis pigmentosa on 6q, determined by homozygosity mapping of chromosomal regions that contain gamma-aminobutyric acid-receptor clusters

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Autosomal dominant Stargardt-like macular dystrophy segregating in a large Canadian family

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A novel locus for Leber congenital amaurosis maps to chromosome 6q

7 January 2021

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A new locus for dominant drusen and macular degeneration maps to chromosome 6q14.

7 January 2021

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A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Interpreting cDNA sequences: some insights from studies on translation

7 January 2021

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Modulation of the fate of cytoplasmic mRNA by AU-rich elements: key sequence features controlling mRNA deadenylation and decay

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy

7 January 2021

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Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa

7 January 2021

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Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13).

7 January 2021

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10.1016/S0006-291X(02)00228-0

7 January 2021

Identifiers

DOI

1 reference

4 November 2017

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