SPTLC1 wt Allele

Known as: LBC1, Hereditary Sensory Neuropathy, Type 1 Gene, LCB1 
Human SPTLC1 wild-type allele is located in the vicinity of 9q22.2 and is approximately 84 kb in length. This allele, which encodes serine… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1996-2018
012319962018

Papers overview

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2014
2014
Mutations in serine palmitoyltransferase long chain subunit 1 (SPTLC1) cause the typical length-dependent axonal degeneration… (More)
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2013
2013
Newly isolated and partially purified trimeric l-methionine-N-carbamoylase from Brevibacillus reuszeri HSN1 was immobilized by… (More)
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2012
2012
The 16S rRNA sequence analysis and biochemical characteristics were confirmed that the isolated bacterium is Pseudomonas sp. LBC1… (More)
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Highly Cited
2010
Highly Cited
2010
HSAN1 is an inherited neuropathy found to be associated with several missense mutations in the SPTLC1 subunit of serine… (More)
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2005
2005
Mutations in enzymes involved in sphingolipid metabolism and trafficking cause a variety of neurological disorders, but details… (More)
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2004
2004
Hereditary sensory neuropathy type I (HSN1) is a common degenerative disorder of peripheral sensory neurons. HSN1 is caused by… (More)
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2002
2002
Hereditary sensory neuropathy type 1 (HSN1) is a dominantly inherited degenerative disorder of the peripheral nerves. HSN1 is… (More)
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Highly Cited
2001
Highly Cited
2001
Hereditary sensory neuropathy type 1 (HSN1, MIM 162400; ref. 1) genetically maps to human chromosome 9q22 (refs. 2–4). We report… (More)
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Highly Cited
2001
Highly Cited
2001
Hereditary sensory neuropathy type I (HSN1) is the most common hereditary disorder of peripheral sensory neurons. HSN1 is an… (More)
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2001
2001
Hereditary sensory neuropathy type I (HSN1) is the most common dominantly inherited degenerative disorder of sensory neurons. The… (More)
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