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USHER SYNDROME, TYPE IC

Known as: USH1C, USHER SYNDROME, TYPE I, ACADIAN VARIETY 
National Institutes of Health

Papers overview

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2011
2011
Purpose This study investigated the genetic basis for Usher syndrome type 1 (USH1) in four consanguineous Israeli Arab families… 
2005
2005
Usher syndrome is characterized by profound hearing loss and retinal degeneration. A splice-site mutation, 216G→A, in exon 3 of… 
2004
2004
Usher syndrome type 1C is an autosomal recessive condition in which profound, congenital sensorineural deafness is found in… 
2001
2001
Abstract. Recently, mutations in USH1C were shown to be associated with Usher syndrome type IC, and a mutation (216G→A) in exon 3… 
1993
1993
The Acadian of southwestern Connecticut exposes a middle crustal level orogenic zone comprised of multiply-deformed metapelitic… 
1989
1989
In the mountainous areas of north-central Maine, the highest peaks are commonly formed in hornfelsic rocks which surround Acadian… 
1981
1981
Peraluminous magmas may be generated by a variety of mechanisms. Isotopic studies can provide strong constraints to be imposed on…