Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome.
Taskiran EZ, Karaosmanoglu B, Koşukcu C, Doğan ÖA, Taylan-Şekeroğlu H, Şimşek-Kiper PÖ, Utine EG, Boduroğlu K, Alikaşifoğlu M.
Taskiran EZ, et al. Among authors: taylan sekeroglu h.
Am J Med Genet A. 2017 Dec;173(12):3143-3152. doi: 10.1002/ajmg.a.38495. Epub 2017 Oct 8.
Am J Med Genet A. 2017.
PMID: 28988429