Lao, Q., Mallappa, A., Rueda Faucz, F., Joyal, E., Veeraraghavan, P., Chen, W., & Merke, D. P. (2020). A TNXB splice donor site variant as a cause of hypermobility type Ehlers–Danlos syndrome in patients with congenital adrenal hyperplasia. Mol Genet Genomic Med.
Stile di citazione ChicagoLao, Qizong, Ashwini Mallappa, Fabio Rueda Faucz, Elizabeth Joyal, Padmasree Veeraraghavan, Wuyan Chen, e Deborah P. Merke. "A TNXB Splice Donor Site Variant As a Cause of Hypermobility Type Ehlers–Danlos Syndrome in Patients With Congenital Adrenal Hyperplasia." Mol Genet Genomic Med 2020.
Citazione MLALao, Qizong, et al. "A TNXB Splice Donor Site Variant As a Cause of Hypermobility Type Ehlers–Danlos Syndrome in Patients With Congenital Adrenal Hyperplasia." Mol Genet Genomic Med 2020.