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pro vyhledávání: '"Pamela B. Fietz"'
Autor:
C. Catharina Müller, Tam H. Nguyen, Barbara Ahlemeyer, Mallika Meshram, Nishreen Santrampurwala, Siyu Cao, Peter Sharp, Pamela B. Fietz, Eveline Baumgart-Vogt, Denis I. Crane
Publikováno v:
Disease Models & Mechanisms, Vol 4, Iss 1, Pp 104-119 (2011)
SUMMARY Delayed cerebellar development is a hallmark of Zellweger syndrome (ZS), a severe neonatal neurodegenerative disorder. ZS is caused by mutations in PEX genes, such as PEX13, which encodes a protein required for import of proteins into the per
Externí odkaz:
https://doaj.org/article/5633aacc1f4d4ca1a76cfcc0e8cca5d4
