TY  - GEN
AU  - Abbasi,Ansar A
AU  - Blaesius,Kathrin
AU  - Hu,Hao
AU  - Latif,Zahid
AU  - Picker-Minh,Sylvie
AU  - Khan,Muhammad N
AU  - Farooq,Sundas
AU  - Khan,Muzammil A
AU  - Kaindl,Angela M
TI  - Identification of a novel homozygous TRAPPC9 gene mutation causing non-syndromic intellectual disability, speech disorder, and secondary microcephaly
SN  - 1552-485X
PY  - 2018///0216
KW  - Adolescent
KW  - Adult
KW  - Carrier Proteins
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - Codon, Nonsense
KW  - Exome
KW  - Female
KW  - Homozygote
KW  - Humans
KW  - Intellectual Disability
KW  - complications
KW  - Intercellular Signaling Peptides and Proteins
KW  - Male
KW  - Microcephaly
KW  - Pedigree
KW  - Prognosis
KW  - Speech Disorders
KW  - Syndrome
KW  - Young Adult
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1002/ajmg.b.32602
ER  -