Ali Hosseini Bereshneh to Pedigree
This is a "connection" page, showing publications Ali Hosseini Bereshneh has written about Pedigree.
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0.255
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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: 0.139
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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: 0.116