Skip to main content
Have a personal or library account? Click to login
Homozygous mutations in ALDH7A1 gene causing pyridoxine dependent epilepsy: Phenotype and genotype of three patients Cover

Homozygous mutations in ALDH7A1 gene causing pyridoxine dependent epilepsy: Phenotype and genotype of three patients

Open Access
|Jun 2025

Authors

Kruti Shah

krutishah96@gmail.com

Faculty of Medicine, Medical College Baroda, Maharaja Sayajirao University, Vadodara,

Shwetal Bhatt

dr_shwetal@yahoo.co.in

Faculty of Medicine, Medical College Baroda, Maharaja Sayajirao University, Vadodara,

Sarbani Raha

drsarbaniraha@rediffmail.com

KGP Children Hospital and Child Neurology and Epilepsy Clinic, Vadodara, Gujarat,
Language: English
Page range: 171 - 174
Published on: Jun 5, 2025
Published by: Sri Lanka College of Paediatricians
In partnership with: Paradigm Publishing Services

© 2025 Kruti Shah, Shwetal Bhatt, Sarbani Raha, published by Sri Lanka College of Paediatricians
This work is licensed under the Creative Commons Attribution 4.0 License.