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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Annals of Neurologyarrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Annals of Neurology
Article . 2004 . Peer-reviewed
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A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese family

Authors: Jean-Baptiste, Rivière; Dominique J, Verlaan; Masoud, Shekarabi; Ronald G, Lafrenière; Mélanie, Bénard; Vazken M, Der Kaloustian; Zuhayr, Shbaklo; +1 Authors

A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese family

Abstract

AbstractHereditary sensory and autonomic neuropathy (HSAN) type II is an autosomal recessive disorder clinically characterized by distal and proximal sensory loss that is caused by the reduction or absence of peripheral sensory nerves. Recently, a novel gene called HSN2 has been found to be the cause of HSAN type II in five families from Newfoundland and Quebec. Screening of this gene in an HSAN type II Lebanese family showed a 1bp deletion mutation found in a homozygous state in all affected individuals. This novel mutation supports the hypothesis that HSN2 is the causative gene for HSAN type II. Ann Neurol 2004;56:572–575

Keywords

Adult, Family Health, Male, Genetic Linkage, DNA Mutational Analysis, Infant, Newborn, Intracellular Signaling Peptides and Proteins, Infant, Nerve Tissue Proteins, Protein Serine-Threonine Kinases, Minor Histocompatibility Antigens, WNK Lysine-Deficient Protein Kinase 1, Humans, Female, Cysteine, Hereditary Sensory and Autonomic Neuropathies, Lebanon, Frameshift Mutation

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
42
Top 10%
Top 10%
Top 10%
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