Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay-Reference-Cited by-同舟云学术

Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay

Published:2018-07 Issue:7 Volume:20 Page:778-784
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Ansar Muhammad,Riazuddin Saima,Sarwar Muhammad Tahir,Makrythanasis Periklis,Paracha Sohail Aziz,Iqbal Zafar,Khan Jamshed,Assir Muhammad Zaman,Hussain Mureed,Razzaq Attia,Polla Daniel Lôpo,Taj Abid Sohail,Holmgren Asbjørn,Batool Naila,Misceo Doriana,Iwaszkiewicz Justyna,de Brouwer Arjan P.M.,Guipponi Michel,Hanquinet Sylviane,Zoete Vincent,Santoni Federico A.,Frengen Eirik,Ahmed Jawad,Riazuddin Sheikh,van Bokhoven Hans,Antonarakis Stylianos E.

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/gim2017113.pdf

Reference39 articles.

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