Correction to: Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye

Correction to: Journal of Clinical Immunology

10.1007/s10875-024-01759-w

Since the publication of this article we have noticed several errors within the main Table 1 of the manuscript. Four variants were given with different transcript IDs of the same gene. There are also 2 nomenclature errors in the variants of P58 and P117. The necessary corrections have been made in the table below. The errors do not affect the causality of the variants, the results or conclusions reported in the manuscript.

The authors apologize for the error, and regret any inconvenience this may have caused.

The original version has been corrected.

Patient no	Clinical diagnosis (IUIS)	Age	Gender	Consan	Gene	Variant	Transcript ID	Zygosity	Consequence	Novelty
P18	CID	20	F	+	PGM3	c.214G>A p.Gly72Ser	NM_001199917.1 The true RefseqID should be NM_001199919.1	Hom	Missense	Novel
P29	SCID	6 m	F	+	ADA	c.551_555del p.Glu184Glyfs*2 c.241G>A p.Gly81Arg	NM_000022.4 NM_000022.4 The true RefseqID should be NM_001322050 for these variants	Comp. Het	Out of frame/Deletion Missense	Novel rs2065384316
P34	SCID	1	M	+	ADA	c.779A>G p.Glu260Gly	NM_001322050 The true RefseqID should be NM_000022.4 for this variant	Hom	Missense	rs1354071013
P58	SCID	2	M	+	DCLRE1C	c.1633delT p.Glu545AsnfsTer The correct nomenclature of this variant is c.1633del p.Glu545Asnfs*58	NM_001350965.2	Hom	Out of frame/Deletion	Novel
P113	PAD/CVID	7	F	+	CASP8	c.919C>T p.Arg307Trp	NM_001372051.1 The true RefseqID should be NM_001080125.1	Hom	Missense	rs17860424
P117	SCID	1	F	+	RAG1	c.2322G>A p.Arg737His The correct nomenclature of this variant is c.2210G>A p.Arg737His The nucleotide position 2322 refers an old transcript	NM_000448.3	Hom	Missense	rs104894286