All papers authored by Anne-Claire Boschat
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2021
Mahmoud Mikdar 
,
Pedro González-Menéndez ,
Xiaoli Cai,
Yujin Zhang,
Marion Serra,
Abdoul K. Dembele,
Anne-Claire Boschat ,
Sylvia Sanquer,
Cerina Chhuon,
Ida Chiara Guerrera ,
Marc Sitbon ,
Olivier Hermine,
Yves Colin ,
Caroline Le Van Kim ,
Sandrina Kinet
and 5 other authors
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,
Pedro González-Menéndez ,
Xiaoli Cai,
Yujin Zhang,
Marion Serra,
Abdoul K. Dembele,
Anne-Claire Boschat ,
Sylvia Sanquer,
Cerina Chhuon,
Ida Chiara Guerrera ,
Marc Sitbon ,
Olivier Hermine,
Yves Colin ,
Caroline Le Van Kim ,
Sandrina Kinet
and 5 other authors
Upload
Christelle Arrondel,
Sophia Missoury,
Rozemarijn Snoek ,
Julie Patat ,
Giulia Menara,
Bruno Collinet ,
Dominique Liger,
Dominique Durand ,
Olivier Gribouval ,
Olivia Boyer ,
Laurine Buscara,
Gaëlle Martin,
Eduardo Machuca,
Fabien Nevo,
Ewen Lescop
and 22 other authors
,
Julie Patat ,
Giulia Menara,
Bruno Collinet ,
Dominique Liger,
Dominique Durand ,
Olivier Gribouval ,
Olivia Boyer ,
Laurine Buscara,
Gaëlle Martin,
Eduardo Machuca,
Fabien Nevo,
Ewen Lescop
and 22 other authors
Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome
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2017
Daniela A. Braun,
Jia Rao,
Geraldine Mollet ,
David Schapiro,
Marie-Claire Daugeron,
Weizhen Tan,
Olivier Gribouval ,
Olivia Boyer,
Patrick Revy,
Tilman Jobst-Schwan,
Johanna Magdalena Schmidt,
Jennifer A. Lawson,
Denny Schanze ,
Shazia Ashraf,
Jeremy F. P. Ullmann
and 87 other authors
,
David Schapiro,
Marie-Claire Daugeron,
Weizhen Tan,
Olivier Gribouval ,
Olivia Boyer,
Patrick Revy,
Tilman Jobst-Schwan,
Johanna Magdalena Schmidt,
Jennifer A. Lawson,
Denny Schanze ,
Shazia Ashraf,
Jeremy F. P. Ullmann
and 87 other authors
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
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