1. SLC25A13 c.1610_1612delinsAT mutation in an Indian patient and literature review of 79 cases of citrin deficiency for genotype-phenotype associations
   Akella Radha Rama Devi et al, 2018, Gene CrossRef
2. Adult‐onset type II citrullinemia manifested as hepatosteatosis or steatohepatitis: A report of three Chinese cases
   Min Wang et al, 2022, Journal of Digestive Diseases CrossRef
3. Clinical landscape of citrin deficiency: A global perspective on a multifaceted condition
   Jun Kido et al, 2024, Journal of Inherited Metabolic Disease CrossRef
4. Sodium Valproate-induced Adult-onset Type 2 Citrullinemia
   Başak Elçin Ateş et al, 2022, Turkish Journal Of Neurology CrossRef