Megan (University of Colorado School of Medicine) Abbott,
Kevin J. (University of California, San Francisco) Bender,
Andreas (Royal Hospital for Children and University of Glasgow) Brunklaus,
Scott (University of Colorado School of Medicine) Demarest,
Shawn (FamilieSCN2A Foundation) Egan,
Isabel (Boston Children’s Hospital and Harvard Medical School) Haviland,
Jennifer A. (Northwestern University Feinberg School of Medicine) Kearney,
Leah (FamilieSCN2A Foundation) Schust Myers,
Heather E. (Boston Children's Hospital and Harvard Medical School) Olson
e.a.
Cambridge University Press
e druk, 2025
9781009530378
SCN2A-Related Disorders
Specificaties
Paperback, 96 blz.
|
EN
Cambridge University Press |
e druk, 2025
ISBN13: 9781009530378
Rubricering
Onderdeel van serie
Elements in Genetics in Epilepsy
Levertijd ongeveer 7 werkdagen
Samenvatting
This Element provides a review of the clinical features, genetic basis, pathophysiology, pharmacology and treatment of these genetic conditions authored by leading experts in the field and accompanied by perspectives shared by affected families. This title is also available as Open Access on Cambridge Core.
Specificaties
ISBN13:9781009530378
Taal:EN
Bindwijze:Paperback
Aantal pagina's:96
Uitgever:Cambridge University Press