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Links from PMC

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PURA
(L102P)
Single nucleotide variant
(missense variant)
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome
+1 more
GConflicting classifications of pathogenicity
PURA
(F233del)
Microsatellite
(inframe_deletion)
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome
+3 more
GPathogenic/Likely pathogenic