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17p13-p12

A chromosome band present on 17p
National Institutes of Health

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4 relations
Chromosome 17 Short ArmChromosomesEIF5A wt AlleleSHBG wt Allele

Papers overview

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2008
2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa
Objective: Mutations in various genes of the neuromuscular junction cause congenital myasthenic syndrome (CMS). A single… 
2008
2008
congenital myasthenia in North Africa 1293 insG founder mutation is a frequent cause of CHRNE The
1993
1993
Chromosomal localization of 9 KOX zinc finger genes: physical linkages suggest clustering of KOX genes on chromosomes 12, 16, and 19
Nine KOX zinc finger genes were localized on four human chromosomes by in situ hybridization of cDNA probes to metaphase… 
1991
1991
Chromosomal localization of two human zinc finger protein genes, ZNF24 (KOX17) and ZNF29 (KOX26), to 18q12 and 17p13-p12, respectively.
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