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SLC4A11 mutations causative of congenital hereditary endothelial dystrophy (CHED) progressing to Harboyan syndrome in consanguineous Pakistani families

Crossref DOI link: https://doi.org/10.1007/s11033-021-06765-4

Published Online: 2021-10-12

Published Print: 2021-11

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

Authors

Firasat, Sabika https://orcid.org/0000-0003-4959-7832
Dur-e-Shawar,

Khan, Wajid Ali

Sughra, Ume

Nousheen,

Kaul, Haiba

Naz, Shagufta

Noreen, Bushra

Gul, Rutaba

Afshan, Kiran
Funding

Funding for this research was provided by:

Quaid-i-Azam University (University Research Fund 2018-2019)

Higher Education Commission, Pakistan (20-2(10)/ASIP/R&D/HEC/17/000530(CAMB)/18)
License Information

Text and Data Mining valid from 2021-10-12

Version of Record valid from 2021-10-12
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Article History

Received: 18 May 2021

Accepted: 17 August 2021

First Online: 12 October 2021

Declarations

:

: We have no conflict of interest.

: Written informed consent was obtained from all the participants included in this study. Furthermore, it is confirmed that written informed consents were signed by the parents/legally authorized representatives of the subjects of the study, who are all minors.

: Not applicable.

: Bioethical Committee (BEC) of Quaid-i-Azam University, Islamabad, Pakistan approved this study.

: Not applicable.

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