Sahar Bayat

2PUBLICATIONS
6CO-AUTHORS
Developmental genetics (incl. sex determination)Gene mapping
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Journal

Publications (2)

|Jul 01, 2026
Expanding the Phenotype and Genotype Spectrum of a Novel Mutation in Hypomyelinating Leukodystrophy-5 With a Review of the Literature on 42 Cases.

|May 19, 2020
A homozygous missense mutation of WFS1 gene causes Wolfram's syndrome without hearing loss in an Iranian family (a report of clinical heterogeneity).

Shahram Torkamandi, Somaye Rezaei, Reza Mirfakhraie

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Frequent Collaborators

1 joint publications

Reza Mirfakhraie

1 joint publications

Milad Gholami

1 joint publications

Hamidreza Khodadadi

1 joint publications

Mohammadreza Ghazavi