Helm, Benjamin M

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