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Clinical and genetic analyses in syndromic intellectual disability with primary microcephaly reveal biallelic and de novo variants in patients with parental consanguinity

Crossref DOI link: https://doi.org/10.1007/s13258-022-01344-8

Published Online: 2022-11-12

Published Print: 2023-01

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Mercan, Sevcan

Akcakaya, Nihan Hande https://orcid.org/0000-0001-8414-4017
Salman, Baris https://orcid.org/0000-0002-7657-8576
Yapici, Zuhal

Ozbek, Ugur https://orcid.org/0000-0001-7031-3932
Ugur Iseri, Sibel Aylin https://orcid.org/0000-0002-5790-6853
Funding

Funding for this research was provided by:

Bilimsel Araştirma Projeleri Birimi, Istanbul Üniversitesi (TDK-2017-25704, TSA-2018-27512)

Türkiye Bilimler Akademisi (GEBIP 2019)
License Information

Text and Data Mining valid from 2022-11-12

Version of Record valid from 2022-11-12
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Article History

Received: 3 August 2022

Accepted: 6 November 2022

First Online: 12 November 2022

Declarations

:

: Sevcan Mercan, Nihan Hande Akcakaya, Baris Salman, Zuhal Yapici, Ugur Ozbek and Sibel Aylin Ugur Iseri declare that they have no conflict of interest.

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