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O’Donnell-Luria, Anne H.;
Pais, Lynn S.;
Faundes, Víctor;
Wood, Jordan C.;
Sveden, Abigail;
Luria, Victor;
Abou Jamra, Rami;
Accogli, Andrea;
Amburgey, Kimberly;
Anderlid, Britt Marie;
Azzarello-Burri, Silvia;
Basinger, Alice A.;
Bianchini, Claudia;
Bird, Lynne M.;
Buchert, Rebecca;
Carre, Wilfrid;
Ceulemans, Sophia;
Charles, Perrine;
Cox, Helen;
Culliton, Lisa;
Currò, Aurora;
Demurger, Florence;
Dowling, James J.;
Duban-Bedu, Benedicte;
[...]
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy
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- Media type: E-Article
- Title: Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy
- Contributor: O’Donnell-Luria, Anne H.; Pais, Lynn S.; Faundes, Víctor; Wood, Jordan C.; Sveden, Abigail; Luria, Victor; Abou Jamra, Rami; Accogli, Andrea; Amburgey, Kimberly; Anderlid, Britt Marie; Azzarello-Burri, Silvia; Basinger, Alice A.; Bianchini, Claudia; Bird, Lynne M.; Buchert, Rebecca; Carre, Wilfrid; Ceulemans, Sophia; Charles, Perrine; Cox, Helen; Culliton, Lisa; Currò, Aurora; Demurger, Florence; Dowling, James J.; Duban-Bedu, Benedicte; [...]
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Published:
Elsevier BV, 2019
- Published in: The American Journal of Human Genetics, 104 (2019) 6, Seite 1210-1222
- Language: English
- DOI: 10.1016/j.ajhg.2019.03.021
- ISSN: 0002-9297
- Origination:
- Footnote:
- Access State: Open Access