Severe Neurodevelopmental Phenotype, Diagnostic and Treatment Challenges in Patients with SECISBP2 Deficiency.
Stoupa A, Franca MM, Abdulhadi-Atwan M, Fujisawa H, Korwutthikulrangsri M, Marchand I, Polak G, Beltrand J, Polak M, Kariyawasam D, Liao XH, Raimondi C, Steigerwald C, Abreu NJ, Bauer AJ, Carré A, Taneja C, Mekhoubad AB, Dumitrescu AM.
Stoupa A, et al. Among authors: bauer aj.
Genet Med. 2024 Sep 21:101280. doi: 10.1016/j.gim.2024.101280. Online ahead of print.
Genet Med. 2024.
PMID: 39315526