DNAH5 and primary ciliary dyskinesia: Exome and Sanger sequencings show that the two PCD individuals shared compound heterozygous variants; they were both carriers for a missense variant leading to amino acid exchange in exon 10 of DNAH5, i.e. NM_001369.2(DNAH5):c.1206 T>A; (p.Asn402Lys); rs140782270 (Figure 7A).