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Dive into the research topics of 'Mitochondrial G8292A and C8794T mutations in patients with Niemann‑Pick disease type C'. Together they form a unique fingerprint.- Sort by
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Abbas Masserrat, Fatemeh Sharifpanah, Leila Akbari, Seyed Hasan Tonekaboni, Parvaneh Karimzadeh, Mahmood Reza Asharafi, Safoura Mazrouei, Heinrich Sauer, Massoud Houshmand
Research output: Contribution to journal › Article › peer-review