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SCKL3 gene
Known as:
SCKL3
, Seckel syndrome 3
National Institutes of Health
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2015
2015
Is the novel SCKL3 at 14q23 the predominant Seckel locus?
Kılınç Mo
,
Ninis Vn
,
+5 authors
Tolun A
European Journal of Human Genetics
2015
Corpus ID: 5173183
2003
2003
Is the novel SCKL3 at 14q23 the predominant Seckel locus?
M. Kilinç
,
V. Ninis
,
+5 authors
A. Tolun
European Journal of Human Genetics
2003
Corpus ID: 10077850
Seckel syndrome (SCKL) is a rare disease with wide phenotypic heterogeneity. A locus (SCKL1) has been identified at 3q and…
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