Cited by

• Primary ciliary dyskinesia caused by homozygous mutation in DNAL1, encoding dynein light chain 1.

  Mazor M, Alkrinawi S, Chalifa-Caspi V, Manor E, Sheffield VC, Aviram M, Parvari R. Mazor M, et al. Am J Hum Genet. 2011 May 13;88(5):599-607. doi: 10.1016/j.ajhg.2011.03.018. Epub 2011 Apr 14. Am J Hum Genet. 2011. PMID: 21496787 Free PMC article.
• Variation in DNAH1 may contribute to primary ciliary dyskinesia.

  Imtiaz F, Allam R, Ramzan K, Al-Sayed M. Imtiaz F, et al. BMC Med Genet. 2015 Mar 17;16:14. doi: 10.1186/s12881-015-0162-5. BMC Med Genet. 2015. PMID: 25927852 Free PMC article.
• Population specificity of the DNAI1 gene mutation spectrum in primary ciliary dyskinesia (PCD).

  Ziętkiewicz E, Nitka B, Voelkel K, Skrzypczak U, Bukowy Z, Rutkiewicz E, Humińska K, Przystałowska H, Pogorzelski A, Witt M. Ziętkiewicz E, et al. Respir Res. 2010 Dec 8;11(1):174. doi: 10.1186/1465-9921-11-174. Respir Res. 2010. PMID: 21143860 Free PMC article.
• Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities.

  Castleman VH, Romio L, Chodhari R, Hirst RA, de Castro SC, Parker KA, Ybot-Gonzalez P, Emes RD, Wilson SW, Wallis C, Johnson CA, Herrera RJ, Rutman A, Dixon M, Shoemark A, Bush A, Hogg C, Gardiner RM, Reish O, Greene ND, O'Callaghan C, Purton S, Chung EM, Mitchison HM. Castleman VH, et al. Am J Hum Genet. 2009 Feb;84(2):197-209. doi: 10.1016/j.ajhg.2009.01.011. Epub 2009 Feb 5. Am J Hum Genet. 2009. PMID: 19200523 Free PMC article.
• Linkage analysis localises a Kartagener syndrome gene to a 3.5 cM region on chromosome 15q24-25.

  Geremek M, Zietkiewicz E, Diehl SR, Alizadeh BZ, Wijmenga C, Witt M. Geremek M, et al. J Med Genet. 2006 Jan;43(1):e1. doi: 10.1136/jmg.2005.031526. J Med Genet. 2006. PMID: 16397065 Free PMC article.