Repository of Research and Investigative Information
Shahid Sadoughi University of Medical Sciences
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(2021) Identification of a novel homozygous mutation in bbs10 gene in an iranian family with bardet-biedl syndrome. Avicenna Journal of Medical Biotechnology. pp. 230-233.
(2019) <i>MFSD8</i> gene mutations; evidence for phenotypic heterogeneity. Ophthalmic Genetics. pp. 141-145. ISSN 1381-6810