Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference81 articles.
1. Abdullah AM, El-Mouzan MI, El Shiekh OK, Al Mazyad A (1996) Congenital glucose-galactose malabsorption in Arab children. J Pediatr Gastroenterol Nutr 23(5):561–564. https://doi.org/10.1097/00005176-199612000-00008 (PMID: 8985845)
2. Al-Baradie RS, Chaudhary MW, Burshaid D, Mir A (2016) Unusual case of glucose-galactose malabsorption with infantile neuroaxonal dystrophy. Austin J Clin Neurol 3(2):1093 (ISSN: 2381-9154)
3. Alfadhel M, Tabarki B (2018) SLC19A3 gene defects sorting the phenotype and acronyms: review. Neuropediatrics 49(2):83–92. https://doi.org/10.1055/s-0037-1607191 (Epub 2017 Sep 29. PMID: 28962040)
4. Al Ghamdi AA, Al Shahwan S, Alshibani F, Melaiki B (2018) Recessive mutations in SLC13A5 result in a loss of
citrate transport and cause refractory epilepsy/status epilepticus, developmental delay and progressive
microcephaly. Neurology 90 (15 Supplement) P1.306
5. Al-Khawaga S, AlRayahi J, Khan F, Saraswathi S, Hasnah R, Haris B, Mohammed I, Abdelalim EM, Hussain K (2019) A SLC16A1 mutation in an infant with ketoacidosis and neuroimaging assessment: expanding the clinical spectrum of MCT1 deficiency. Front Pediatr 18(7):299. https://doi.org/10.3389/fped.2019.00299 (PMID: 31380330; PMCID: PMC6657212)
Cited by
12 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献