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SCKL3 gene

Known as: SCKL3, Seckel syndrome 3 
 
National Institutes of Health

Papers overview

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2015
2015
Is the novel SCKL3 at 14q23 the predominant Seckel locus?
 
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2003
2003
Is the novel SCKL3 at 14q23 the predominant Seckel locus?
Seckel syndrome (SCKL) is a rare disease with wide phenotypic heterogeneity. A locus (SCKL1) has been identified at 3q and… Expand
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