Selina H. Banu
Mirpur, C, Bangladesh
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 9 publications
Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy.
Journal: The Journal of clinical investigation
Published: July 08, 2024
The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders.
Journal: Brain : a journal of neurology
Published: October 06, 2023
Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders.
Journal: Brain : a journal of neurology
Published: May 18, 2022
Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly.
Journal: Brain : a journal of neurology
Published: October 15, 2021
Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 05, 2021
Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder.
Journal: American journal of human genetics
Published: June 17, 2019
Correction to: Expanding the genetic heterogeneity of intellectual disability.
Journal: Human genetics
Published: December 31, 2017
Expanding the genetic heterogeneity of intellectual disability.
Journal: Human genetics
Published: July 10, 2017
Prediction of seizure outcome in childhood epilepsies in countries with limited resources: a prospective study.
Journal: Developmental medicine and child neurology
Published: June 12, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026