TY  - GEN
AU  - Powis,Z
AU  - Petrik,I
AU  - Cohen,J S
AU  - Escolar,D
AU  - Burton,J
AU  - van Ravenswaaij-Arts,C M A
AU  - Sival,D A
AU  - Stegmann,A P A
AU  - Kleefstra,T
AU  - Pfundt,R
AU  - Chikarmane,R
AU  - Begtrup,A
AU  - Huether,R
AU  - Tang,S
AU  - Shinde,D N
TI  - De novo variants in KLF7 are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms
SN  - 1399-0004
PY  - 2019///0925
KW  - Adolescent
KW  - Autism Spectrum Disorder
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - Developmental Disabilities
KW  - Female
KW  - Genetic Predisposition to Disease
KW  - Haploinsufficiency
KW  - Humans
KW  - Intellectual Disability
KW  - Kruppel-Like Transcription Factors
KW  - Male
KW  - Mutation, Missense
KW  - Exome Sequencing
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1111/cge.13198
ER  -