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2021 | 1 |
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Novel STAMBP mutation and additional findings in an Arabic family.
Am J Med Genet A. 2015 Apr;167A(4):805-9. doi: 10.1002/ajmg.a.36782. Epub 2015 Feb 18.
Am J Med Genet A. 2015.
PMID: 25692795
Clinical and Molecular Characteristics of Neuronal Ceroid Lipofuscinosis in Saudi Arabia.
Saleh MM, Hamhom AM, Al-Otaibi A, AlGhamdi M, Housawi Y, Aljadhai YI, Alameer S, Almannai M, Jad LA, Alwadei AH, Tabassum S, Alsaman A, AlAsmari A, Al Mutairi F, Althiyab H, Bashiri FA, AlHumaidi S, Alfadhel M, Mink JW, AlHashim A, Faqeih EA; Saudi NCL Study Consortium.
Saleh MM, et al.
Pediatr Neurol. 2024 Mar 7;155:149-155. doi: 10.1016/j.pediatrneurol.2024.03.004. Online ahead of print.
Pediatr Neurol. 2024.
PMID: 38653183
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Clinical and molecular characteristics of primary ciliary dyskinesia: A tertiary care centre experience.
Alzaid M, Al-Mobaireek K, Almannai M, Mukhtar G, Eltahir S, Zafar A, Zada AP, Alotaibi W.
Alzaid M, et al. Among authors: zada ap.
Int J Pediatr Adolesc Med. 2021 Dec;8(4):258-263. doi: 10.1016/j.ijpam.2021.03.002. Epub 2021 Mar 11.
Int J Pediatr Adolesc Med. 2021.
PMID: 34401452
Free PMC article.
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