Fig 4
From: Mutations causing severe combined immunodeficiency: detection with a custom resequencing microarray
Discovery of IL2RG exon 5 missense 684C>T; R224W variant. A, Variant T first identified by resequencing with array, highlighted in green. B, Variant, confirmed by dideoxy sequencing. This was a new mutation in the patient; DNA derived from maternal blood had only reference sequence.
