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Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability.更正:对巴基斯坦近亲家庭进行外显子组测序,确定了30个导致隐性智力残疾的新候选基因。
Mol Psychiatry. 2020 Nov;25(11):3101-3102. doi: 10.1038/s41380-018-0128-z.
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引用本文的文献

1
Congenital cataract: An ocular manifestation of classical homocystinuria.先天性白内障:经典同型胱氨酸尿症的眼部表现。
Mol Genet Genomic Med. 2021 Sep;9(9):e1742. doi: 10.1002/mgg3.1742. Epub 2021 Aug 2.

更正:对巴基斯坦近亲家庭进行外显子组测序,确定了30个导致隐性智力残疾的新候选基因。

Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability.

作者信息

Riazuddin S, Hussain M, Razzaq A, Iqbal Z, Shahzad M, Polla D L, Song Y, van Beusekom E, Khan A A, Tomas-Roca L, Rashid M, Zahoor M Y, Wissink-Lindhout W M, Basra M A R, Ansar M, Agha Z, van Heeswijk K, Rasheed F, Van de Vorst M, Veltman J A, Gilissen C, Akram J, Kleefstra T, Assir M Z, Grozeva D, Carss K, Raymond F L, O'Connor T D, Riazuddin S A, Khan S N, Ahmed Z M, de Brouwer A P M, van Bokhoven H, Riazuddin S

机构信息

Department of Otorhinolaryngology-Head and Neck Surgery, University of Maryland, School of Medicine, Baltimore, MD, USA.

Center for Genetic Diseases, Shaheed Zulfiqar Ali Bhutto Medical University, Pakistan Institute of Medical Sciences, Islamabad, Pakistan.

出版信息

Mol Psychiatry. 2020 Nov;25(11):3101-3102. doi: 10.1038/s41380-018-0128-z.

DOI:10.1038/s41380-018-0128-z
PMID:
30171209
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7962566/
Abstract

This Article was originally published under a CC BY-NC-SA 4.0 license, but has now been made available under a CC BY 4.0 license. The PDF and HTML versions of the Article have been modified accordingly.

摘要

本文最初以知识共享署名-非商业性使用-相同方式共享 4.0 许可协议发布,但现在已根据知识共享署名 4.0 许可协议提供。文章的 PDF 和 HTML 版本已相应修改。