De novo apparent loss-of-function mutations in PRR12 in three patients with intellectual disability and iris abnormalities
Leduc, Magalie S., Mcguire, Marianne, Madan-Khetarpal, Suneeta, Ortiz, Damara, Hayflick, Susan, Keller, Kory, Eng, Christine M., Yang, Yaping, Bi, WeiminLanguage:
english
Journal:
Human Genetics
DOI:
10.1007/s00439-018-1877-0
Date:
March, 2018
File:
PDF, 1.25 MB
english, 2018