Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical),Biochemistry
Reference31 articles.
1. Aryani O, Manshadi MD, Tondar M, Khalili E, Kamalidehghan B, Ahmadipour F, Fani S, Houshmand M (2014) A newly identified c. 1824_1828dupATACG mutation in exon 13 of the GAA gene in infantile-onset glycogen storage disease type II (Pompe disease). Mol Biol Rep 41:6211–6214
2. Bahreini F, Houshmand M, Modaresi MH, Tonekaboni H, Nafissi S, Nazari F, Akrami SM (2016) Mitochondrial copy number and D-loop variants in pompe patients. Cell J (Yakhteh) 18:405
3. Benz k, Hahn p, Hanisch m, Lücke k, Lücke t, Jackowski j (2019) Systematic review of oral and craniofacial findings in patients with Fabry disease or Pompe disease. Br J Oral Maxillofac Surg 57:831–838
4. Bosman L, Hoeks SE, González Candel A, Van Den Hout HJ, Van Der Ploeg AT, Staals LM (2018) Perioperative management of children with glycogen storage disease type II—Pompe disease. Pediatr Anesth 28:428–435
5. Chojnacki S, Cowley A, Lee J, Foix A, Lopez R (2017) Programmatic access to bioinformatics tools from EMBL-EBI update: 2017. Nucleic Acids Res 45:W550–W553
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