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2p22-p21

A chromosome band present on 2p
National Institutes of Health

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6 relations
BIRC6 wt AlleleChromosome 2 Short ArmChromosomesEIF2AK2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutation
SPG4 or SPAST-associated hereditary spastic paraplegia (HSP) is an autosomal dominant (AD) disorder characterized by… 
2005
2005
Large deletion involving the 5′‐UTR in the spastin gene caused mild phenotype of autosomal dominant hereditary spastic paraplegia
Hereditary spastic paraplegia (HSP) due to mutations in the spastin gene (SPG4) located to 2p22‐p21 is the most common form of… 
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