Jalilolghadr S
No ORCID on file
· 1 paper in corpus
· active 2023
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Frequent coauthors
- Alizadeh M 1
- Ghodsi M 1
- Saffari F 1
- Taremiha A 1
2023
Alstrom syndrome is a rare genetic disorder with an autosomal recessive mutation in the ALMS1 gene. The disease's manifestations include ophthalmic problems, hearing loss, obesity, and cardiovascular disorders. In addition, medical cases in…