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USH1A: chronicle of a slow death
scientific article
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scholarly article
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title
USH1A: chronicle of a slow death
(English)
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author
Sylvie Gerber
series ordinal
1
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Arnold Munnich
series ordinal
4
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Jean-Michel Rozet
series ordinal
6
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Josseline Kaplan
series ordinal
7
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Jean-Louis Dufier
series ordinal
5
object named as
Jean-Louis Dufier
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author name string
Dominique Bonneau
series ordinal
2
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Brigitte Gilbert
series ordinal
3
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language of work or name
English
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publication date
February 2006
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published in
American Journal of Human Genetics
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volume
78
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issue
2
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page(s)
357-9
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cites work
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Identification and cloning of the human homolog (JAG1) of the rat Jagged1 gene from the Alagille syndrome critical region at 20p12
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24 March 2017
Isolation of a novel human homologue of the gene coding for echinoderm microtubule-associated protein (EMAP) from the Usher syndrome type 1a locus at 14q32
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24 March 2017
Defective myosin VIIA gene responsible for Usher syndrome type 1B
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24 March 2017
Cloning and genetic characterization of the human kinesin light-chain (KLC) gene
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Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
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24 March 2017
A gene for Usher syndrome type I (USH1A) maps to chromosome 14q
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Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population
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27 September 2017
Characterization, chromosomal localization, and the complete 30-kb DNA sequence of the human Jagged2 (JAG2) gene.
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Genetic heterogeneity of Bardet-Biedl syndrome in a distinct Canadian population: evidence for a fifth locus
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Usher's syndrome. Ophthalmic and neuro-otologic findings suggesting genetic heterogeneity
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Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneity.
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30 May 2018
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Genetic heterogeneity in Usher syndrome
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12 December 2020
based on heuristic
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Identifiers
DOI
10.1086/500275
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PMCID
1380243
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PubMed ID
16400615
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ResearchGate publication ID
7370498
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