Genetics in Medicine Open (Jan 2024)
P153: Characterizing the spectrum of CACNA1A-related disorders*
- Emile Moura Coelho da Silva,
- Alina Ivaniuk,
- Emily Huth,
- Costin Leu,
- Oscar Mancera,
- Omolara Kolawole,
- Matthew Wright,
- Ian Butler,
- Pauline Filipek,
- Jeremy Lankford,
- Michael Watkins,
- Elia Pestana Knight,
- Samden Lhatoo,
- Gretchen Von Allmen,
- Dennis Lal
Affiliations
- Emile Moura Coelho da Silva
- Department of Neurology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, Center for Neurogenetics, The University of Texas Health Science Center at Houston, Houston, TX
- Alina Ivaniuk
- Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, OH
- Emily Huth
- Department of Neurology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, Center for Neurogenetics, The University of Texas Health Science Center at Houston, Houston, TX
- Costin Leu
- Department of Neurology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, Center for Neurogenetics, The University of Texas Health Science Center at Houston, Houston, TX, Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, OH
- Oscar Mancera
- Department of Neurology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX
- Omolara Kolawole
- Department of Neurology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX
- Matthew Wright
- Department of Neurology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX
- Ian Butler
- Division of Child and Adolescent Neurology, Department of Pediatrics, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX
- Pauline Filipek
- Division of Child and Adolescent Neurology, Department of Pediatrics, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX
- Jeremy Lankford
- Department of Neurology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, Division of Child and Adolescent Neurology, Department of Pediatrics, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX
- Michael Watkins
- Division of Child and Adolescent Neurology, Department of Pediatrics, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX
- Elia Pestana Knight
- Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, OH
- Samden Lhatoo
- Department of Neurology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, Texas Institute for Restorative Neurotechnologies, The University of Texas Health Science Center at Houston, Houston, TX
- Gretchen Von Allmen
- Department of Neurology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, Division of Child and Adolescent Neurology, Department of Pediatrics, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX
- Dennis Lal
- Department of Neurology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, Center for Neurogenetics, The University of Texas Health Science Center at Houston, Houston, TX, Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, OH, Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, Cologne Center for Genomics (CCG), University of Cologne, Cologne, DE
- Journal volume & issue
-
Vol. 2
p. 101050
