The role of IQSEC2 in syndromic intellectual disability: Narrowing the diagnostic odyssey. [electronic resource]
- American journal of medical genetics. Part A Oct 2017
- 2814-2820 p. digital
Publication Type: Case Reports; Journal Article
1552-4833
10.1002/ajmg.a.38404 doi
Adolescent Adult Child Female Guanine Nucleotide Exchange Factors--genetics Humans Infant Intellectual Disability--diagnosis Male Mutation Prognosis Syndrome Young Adult