Résultats de la recherche - Mihaela Pupavac
- Résultat(s) 1 - 3 résultats de 3
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1
Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities par Anita M. Quintana, Hung‐Chun Yu, Alison Brebner, Mihaela Pupavac, Elizabeth A. Geiger, Abigail Watson, Victoria L. Castro, Warren Cheung, Shu‐Huang Chen, David Watkins, Tomi Pastinen, Flemming Skovby, Bruce Appel, David S. Rosenblatt, Tamim H. Shaikh
Publié 2017Artigo -
2
Matchmaking facilitates the diagnosis of an autosomal-recessive mitochondrial disease caused by biallelic mutation of the tRNA isopentenyltransferase (<i>TRIT1</i> ) gene par Kristin D. Kernohan, David A. Dyment, Mihaela Pupavac, Zvi Cramer, Arran McBride, Geneviève Bernard, Isabella R. Straub, Martine Tétreault, Taila Hartley, Lijia Huang, Erick Sell, Jacek Majewski, David S. Rosenblatt, Eric A. Shoubridge, Aziz Mhanni, Tara Myers, Virginia K. Proud, S. Schrier Vergano, Brooke Spangler, Emily Farrow, Jennifer Kussman, Nicole P. Safina, Carol Saunders, Kym M. Boycott, Isabelle Thiffault
Publié 2017Artigo -
3
A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients par Jean‐Louis Guéant, Céline Chéry, Abderrahim Oussalah, Javad Nadaf, David Coelho, Thomas Josse, Justine Flayac, Aurélie Robert, Isabelle Koscinski, Isabelle Gastin, Pierre Filhine-Trésarrieu, Mihaela Pupavac, Alison Brebner, David Watkins, Tomi Pastinen, Alexandre Montpetit, Fadi Hariri, David‐Alexandre Trégouët, Benjamin A. Raby, Wendy K. Chung, Pierre‐Emmanuel Morange, D. Sean Froese, Matthias R. Baumgartner, Jean‐François Benoist, Can Fıçıcıoğlu, Virginie Marchand, Yuri Motorin, C. Bonnemains, François Feillet, Jacek Majewski, David S. Rosenblatt
Publié 2017Artigo