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

Published Print: 2018-07

Authors

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.
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This article is maintained by: Elsevier

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

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/gim.2017.113

Content Type: article

Copyright: © 2018, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics

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