Ali Hosseini Bereshneh to Child, Preschool
This is a "connection" page, showing publications Ali Hosseini Bereshneh has written about Child, Preschool.
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0.160
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Crystallographic modeling of the PNPT1:c.1453A>G variant as a cause of mitochondrial dysfunction and autosomal recessive deafness; expanding the neuroimaging and clinical features. Mitochondrion. 2021 07; 59:1-7.
Score: 0.058
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Expanding the clinical and neuroimaging features of NKX6-2-related hereditary spastic ataxia type 8. Eur J Med Genet. 2020 May; 63(5):103868.
Score: 0.054
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Novel in-frame deletion in MFSD8 gene revealed by trio whole exome sequencing in an Iranian affected with neuronal ceroid lipofuscinosis type 7: a case report. J Med Case Rep. 2018 Sep 25; 12(1):281.
Score: 0.049