Genetic background of FHLH in Qatar: Registry data and population study
Elkhansa Elgaali(Qatar Airways (Qatar)), Chiara Cugno(Qatar Airways (Qatar)), Aesha I. Ali, Naima Al-Mulla(Qatar Airways (Qatar)), Tawfeg Ben‐Omran(Qatar Airways (Qatar)), Massimo Mezzavilla(University of Padua), Ghada Abdelaziz, Ayman Saleh(Horiba (Japan)), Mohammed Elanbari(Sidra Medical and Research Center), Ikhlak Ahmed, Khalid A. Fakhro(Sidra Medical and Research Center)
Cited by 0
Related Papers
Nusinersen initiated in infants during the presymptomatic stage of spinal muscular atrophy: Interim efficacy and safety results from the Phase 2 NURTURE study
|Neuromuscular Disorders|2019|636
Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders
|Science|2014|548
Guidelines for the diagnosis and management of cystathionine beta‐synthase deficiency
|Journal of Inherited Metabolic Disease|2016|335