NIPAL4 gene

Known as: ICHTHYIN, NIPAL4, NIPA-LIKE DOMAIN-CONTAINING 4 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1982-2018
012319822018

Papers overview

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2017
2017
Autosomal recessive congenital ichthyosis in the American bulldog is characterized by generalized scaling and erythema with… (More)
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2015
2015
A minority of patients with nonsyndromic autosomal recessive congenital ichthyosis (ARCI) display mutations in NIPAL4 (ICHTHYIN… (More)
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2012
2012
Autosomal recessive congenital ichthyosis (ARCI) is a heterogeneous group of skin barrier diseases due inter alia to mutations in… (More)
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2012
2012
Autosomal recessive congenital ichthyosis (ARCI) is a group of disorders characterized by abnormal desquamation of the skin and a… (More)
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2012
2012
Ichthyosis is a heterogeneous disorder characterized by abnormal skin scaling over the whole body. Autosomal recessive congenital… (More)
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2011
2011
BACKGROUND   Mutations in six genes have been identified in autosomal recessive congenital ichthyosis (ARCI). To date, few… (More)
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2009
2009
Lamellar ichthyosis is a keratinization disorder caused by TGM1, Ichthyin and several other gene mutations. A new treatment… (More)
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Highly Cited
2007
Highly Cited
2007
To understand the functions of NIPA1, mutated in the neurodegenerative disease hereditary spastic paraplegia, and of ichthyin… (More)
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2007
2007
BACKGROUND Autosomal recessive congenital ichthyosis (ARCI) is a heterogeneous group of skin disorders. Several mutant genes have… (More)
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Highly Cited
2004
Highly Cited
2004
We report the genomic localization by homozygosity mapping and the identification of a gene for a new form of non-syndromic… (More)
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