ERCC6 and Cerebellar atrophy: In patient 011 with a T−B+NK− SCID phenotype associated with deafness, microcephaly, brain and cerebellar atrophy, developmental delay, NGS revealed 2 heterozygous mutations of ADA gene, located in the same allele, the first one being likely pathogenic, and a further heterozygous variant of unknown significance of ERCC6 gene.