USH1G wt Allele

Known as: ANKS4A, Usher Syndrome 1G (Autosomal Recessive) wt Allele, FLJ33924 
Human USH1G wild-type allele is located in the vicinity of 17q25.1 and is approximately 7 kb in length. This allele, which encodes Usher syndrome… (More)
National Institutes of Health

Papers overview

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2014
2014
Surgical site infections (SSI) are a significant cause of post-surgical morbidity and mortality and can be an indicator of… (More)
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Highly Cited
2012
Highly Cited
2012
OBJECTIVES The World Health Organization considers Cesarean section rates of 5-15% to be the optimal range for targeted provision… (More)
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2011
2011
Usher syndrome (USH) is the most frequent cause of combined deaf-blindness in man. An important finding from mouse models and… (More)
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2010
2010
To the Editor : Usher syndrome is an autosomal, recessively inherited disorder involving progressive retinitis pigmentosa and… (More)
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2007
2007
The sentence in lines 3–5 of the third page of the article (“Materials and methods” section) was incorrectly rendered as… (More)
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2006
2006
  • 2006
I examine the role of humanitarianism and compassion in an emergent ethical configuration that makes illness a primary means by… (More)
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Highly Cited
2005
Highly Cited
2005
Defects in myosin VIIa, harmonin (a PDZ domain protein), cadherin 23, protocadherin 15 and sans (a putative scaffolding protein… (More)
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1991
1991
We show that the dimension of an algebraic (a ne or projective) variety can be computed by a well parallelizable arithmetical… (More)
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1974
1974
The present communication described changes on nerve biopsies from 16 diabetics without neuropathy, except the fact that the… (More)
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