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CLDN14 gene

Known as: CLAUDIN 14, CLDN14 
National Institutes of Health

Related topics

Related topics

1 relation
claudin 14 protein

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Variantes alélicas raras en la enfermedad de Ménière: De los casos familiares a los casos esporádicos
espanolResumen La enfermedad de Meniere [EM;MIM 156000] es un trastorno cronico caracterizado por ataques de vertigo asociados a… 
2018
2018
Genetic analysis of CLDN14 in the Chinese population affected with non-syndromic hearing loss.
2016
2016
A Common Variant in CLDN14 is Associated with Primary Biliary Cirrhosis and Bone Mineral Density
Primary biliary cirrhosis (PBC), a chronic autoimmune liver disease, has been associated with increased incidence of osteoporosis… 
2016
2016
A Novel Common Variant in CLDN14 is Associated with Primary Biliary Cirrhosis
2013
2013
Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss.
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