First insights into genotype and phenotype of familial amyotrophic lateral sclerosis in Egypt: early onset and high consanguinity
Front Med
.
2024 Oct 12.
doi: 10.1007/s11684-024-1100-8.
Online ahead of print.
Authors
Nabila Hamdi
1
,
Kathrin Mueller
2
,
Amr Hamza
3
,
Radwa Soliman
4
,
Enass Onbool
4
,
Kareem Omran
4
,
Omnia Ocab
3
,
Axel Freischmidt
5
,
Reiner Siebert
2
,
Albert Ludolph
5
6
,
Nagia Fahmy
4
Affiliations
1
Molecular Pathology Unit, The German University in Cairo, New Cairo City, 11835, Egypt. nabila.hamdi@guc.edu.eg.
2
Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, 89081, Germany.
3
Molecular Pathology Unit, The German University in Cairo, New Cairo City, 11835, Egypt.
4
Neuromuscular Unit, Faculty of Medicine, Ain Shams University, Cairo, 11591, Egypt.
5
Department of Neurology, Ulm University, Ulm, 89081, Germany.
6
German Center for Neurodegenerative Diseases (DZNE), Ulm Site, Ulm, 89081, Germany.
PMID:
39397192
DOI:
10.1007/s11684-024-1100-8
No abstract available
Publication types
Letter