Associated Papers
Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease.
Keller N et al.
Human Mutation, 2021
Investigation of ITGB2 gene in 12 new cases of leukocyte adhesion deficiency-type I revealed four novel mutations from Iran.
Taghizade Mortezaee F et al.
Archives of Iranian Medicine, 2015
Characterization of 11 new cases of leukocyte adhesion deficiency type 1 with seven novel mutations in the ITGB2 gene.
Parvaneh N et al.
Journal of Clinical Immunology, 2010
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