Primary ciliary dyskinesia-kartagener syndrome in a family with a novel DNAH5 gene mutation and variable phenotypes
By: Marafi, Makia J.; al-Sulayman, Ibrahim S.; Rida, Abd Allah M.…[et al.]. The Egyptian Journal of Medical Human Genetics. Vol. 16, no. 1 (2015), pp.95-99, 5 p.
Subjects: Kuwait; Diagnosis; Health aspects