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Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder

Crossref DOI link: https://doi.org/10.1038/s41436-021-01133-w

Published Print: 2021-07

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Polla, Daniel L.

Farazi Fard, Mohammad Ali

Tabatabaei, Zahra

Habibzadeh, Parham

Levchenko, Olga A.

Nikuei, Pooneh

Makrythanasis, Periklis

Hussain, Mureed

von Hardenberg, Sandra

Zeinali, Sirous

Fallah, Mohammad-Sadegh

Schuurs-Hoeijmakers, Janneke H.M.

Shahzad, Mohsin

Fatima, Fareeha

Fatima, Neelam

Kaat, Laura Donker

Bruggenwirth, Hennie T.

Fleming, Leah R.

Condie, John

Ploski, Rafal

Pollak, Agnieszka

Pilch, Jacek

Demina, Nina A.

Chukhrova, Alena L.

Sergeeva, Vasilina S.

Venselaar, Hanka

Masri, Amira T.

Hamamy, Hanan

Santoni, Federico A.

Linda, Katrin

Ahmed, Zubair M.

Nadif Kasri, Nael

de Brouwer, Arjan P.M.

Bergmann, Anke K.

Hethey, Sven

Yavarian, Majid

Ansar, Muhammad

Riazuddin, Saima

Riazuddin, Sheikh

Silawi, Mohammad

Ruggeri, Gaia

Pirozzi, Filomena

Eftekhar, Ebrahim

Taghipour Sheshdeh, Afsaneh

Bahramjahan, Shima

Mirzaa, Ghayda M.

Lavrov, Alexander V.

Antonarakis, Stylianos E.

Faghihi, Mohammad Ali

van Bokhoven, Hans
Funding

Funding for this research was provided by:

EU FP7 Large-Scale Integrating Project Genetic and Epigenetic Networks in Cognitive Dysfunction (241995, 241995)
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This article is maintained by: Elsevier

Article Title: Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-021-01133-w

Content Type: article

Copyright: © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics

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