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Loss of function of SVBP leads to autosomal recessive intellectual disability, microcephaly, ataxia, and hypotonia

Crossref DOI link: https://doi.org/10.1038/s41436-018-0415-8

Published Print: 2019-08

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

Authors

Iqbal, Zafar

Tawamie, Hasan

Ba, Wei

Reis, André

Halak, Bassam Al

Sticht, Heinrich

Uebe, Steffen

Kasri, Nael Nadif

Riazuddin, Sheikh

van Bokhoven, Hans

Abou Jamra, Rami
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Text and Data Mining valid from 2019-08-01

Text and Data Mining valid from 2019-08-01

Version of Record valid from 2022-01-19
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This article is maintained by: Elsevier

Article Title: Loss of function of SVBP leads to autosomal recessive intellectual disability, microcephaly, ataxia, and hypotonia

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-018-0415-8

Content Type: article

Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics