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Case Report
Peer-Review Record

Genotype–Phenotype Correlation Model for the Spectrum of TYR-Associated Albinism

Diagnostics 2024, 14(15), 1583; https://doi.org/10.3390/diagnostics14151583
by Mirjana Bjeloš 1,2,3, Ana Ćurić 1,3,*, Mladen Bušić 1,2,3, Benedict Rak 1 and Biljana Kuzmanović Elabjer 1,2,3
Reviewer 1:
Reviewer 2: Anonymous
Diagnostics 2024, 14(15), 1583; https://doi.org/10.3390/diagnostics14151583
Submission received: 16 June 2024 / Revised: 16 July 2024 / Accepted: 22 July 2024 / Published: 23 July 2024
(This article belongs to the Special Issue Diagnosis, Treatment and Management of Eye Diseases, Second Edition)

Round 1

Reviewer 1 Report

Comments and Suggestions for Authors

Please see comments file attached.

Comments for author File: Comments.pdf

Comments on the Quality of English Language


Author Response

Please see the attachment.

Author Response File: Author Response.pdf

Reviewer 2 Report

Comments and Suggestions for Authors

Line 203: “The variant was found at a frequency of 0.2465, …” How is this frequency expressed, in Hz? Is the number of significant digits correct?

For the imaging of patients, you relied on the Optos wide field imaging with FAF and on OCT. Given how melanin plays a big role in this research, how useful are these machines in determining melanin? Would standard fundus photography be more appropriate?

Author Response

Please see the attachment.

Author Response File: Author Response.pdf

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