Dalal K. Bubshait. (2023). Novel PTRH2 gene variant causing IMNEPD (infantile-onset multisystem neurologic, endocrine, and pancreatic disease) in 2 Saudi siblings. The Korean Pediatric Society.
Chicago Style (17th ed.) CitationDalal K. Bubshait. Novel PTRH2 Gene Variant Causing IMNEPD (infantile-onset Multisystem Neurologic, Endocrine, and Pancreatic Disease) in 2 Saudi Siblings. The Korean Pediatric Society, 2023.
MLA (9th ed.) CitationDalal K. Bubshait. Novel PTRH2 Gene Variant Causing IMNEPD (infantile-onset Multisystem Neurologic, Endocrine, and Pancreatic Disease) in 2 Saudi Siblings. The Korean Pediatric Society, 2023.
Warning: These citations may not always be 100% accurate.