Alexis A. Jourdain
AuthID: R-00H-BH8
1
TÃTULO: Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies
AUTORES: Rene G Feichtinger; Monika Olahova; Yoshihito Kishita; Caterina Garone; Laura S Kremer; Mikako Yagi; Takeshi Uchiumi; Alexis A Jourdain; Kyle Thompson; Aaron R D'Souza; Robert Kopajtich; Charlotte L Alston; Johannes Koch; Wolfgang Sperl; Elisa Mastantuono; Tim M Strom; Saskia B Wortmann; Thomas Meitinger; Germaine Pierre; Patrick F Chinnery; ...Mais
PUBLICAÇÃO: 2017, FONTE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 101, NÚMERO: 4
AUTORES: Rene G Feichtinger; Monika Olahova; Yoshihito Kishita; Caterina Garone; Laura S Kremer; Mikako Yagi; Takeshi Uchiumi; Alexis A Jourdain; Kyle Thompson; Aaron R D'Souza; Robert Kopajtich; Charlotte L Alston; Johannes Koch; Wolfgang Sperl; Elisa Mastantuono; Tim M Strom; Saskia B Wortmann; Thomas Meitinger; Germaine Pierre; Patrick F Chinnery; ...Mais
PUBLICAÇÃO: 2017, FONTE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 101, NÚMERO: 4
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