TY  - GEN
AU  - Ansar,Muhammad
AU  - Riazuddin,Saima
AU  - Sarwar,Muhammad Tahir
AU  - Makrythanasis,Periklis
AU  - Paracha,Sohail Aziz
AU  - Iqbal,Zafar
AU  - Khan,Jamshed
AU  - Assir,Muhammad Zaman
AU  - Hussain,Mureed
AU  - Razzaq,Attia
AU  - Polla,Daniel Lôpo
AU  - Taj,Abid Sohail
AU  - Holmgren,Asbjørn
AU  - Batool,Naila
AU  - Misceo,Doriana
AU  - Iwaszkiewicz,Justyna
AU  - de Brouwer,Arjan P M
AU  - Guipponi,Michel
AU  - Hanquinet,Sylviane
AU  - Zoete,Vincent
AU  - Santoni,Federico A
AU  - Frengen,Eirik
AU  - Ahmed,Jawad
AU  - Riazuddin,Sheikh
AU  - van Bokhoven,Hans
AU  - Antonarakis,Stylianos E
TI  - Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay
SN  - 1530-0366
PY  - 2018///1211
KW  - Alleles
KW  - Chromosome Mapping
KW  - methods
KW  - Family
KW  - Female
KW  - Gene Frequency
KW  - genetics
KW  - Genotype
KW  - Homozygote
KW  - Humans
KW  - Intellectual Disability
KW  - Language Development Disorders
KW  - Male
KW  - Membrane Proteins
KW  - Microcephaly
KW  - Motor Activity
KW  - Mutation, Missense
KW  - Nerve Tissue Proteins
KW  - Pakistan
KW  - Pedigree
KW  - Phenotype
KW  - Sequence Analysis, Protein
KW  - Exome Sequencing
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/gim.2017.113
ER  -