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of 3
pro vyhledávání: '"Kayla Clokie"'
Autor:
Marie-Claude Beauchamp, Anissa Djedid, Kevin Daupin, Kayla Clokie, Shruti Kumar, Jacek Majewski, Loydie Anne Jerome-Majewska
Publikováno v:
PLoS ONE, Vol 14, Iss 7, p e0219280 (2019)
Mutations in EFTUD2 are responsible for the autosomal dominant syndrome named MFDM (mandibulofacial dysostosis with microcephaly). However, it is not clear how reduced levels of EFTUD2 cause abnormalities associated with this syndrome. To determine i
Externí odkaz:
https://doaj.org/article/412905e3589f4083b86131b0c47d5a1e
Autor:
Marie-Claude Beauchamp, Loydie Jerome Majewska, Jacek Majewski, Anissa Djedid, Kayla Clokie, Kevin Daupin
Publikováno v:
The FASEB Journal. 33
Autor:
Marie-Claude Beauchamp, Sabrina Shameen Alam, Anissa Djedid, Kayla Clokie, Shruti Kumar, Jacek Majewski, Loydie A. Jerome-Majewska, Kevin Daupin
Publikováno v:
The FASEB Journal. 33