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HE Shamseldin

First name:
HE
Last name:
Shamseldin
Almannai, M., Alsamri, A., Alqasmi, A., Faqeih, E., AlMutairi, F., Alotaibi, M., … Alkuraya, F. (2018). Expanding the phenotype of SLC25A42-associated mitochondrial encephalomyopathy. Clinical Genetics. https://doi.org/10.1111/cge.13210 (Original work published 2018)
Wagner, M., Skorobogatko, Y., Pode-Shakked, B., Powell, C., Alhaddad, B., Seibt, A., … Distelmaier, F. (2020). Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities. American Journal of Human Genetics, 106(2), 246-255. https://doi.org/10.1016/j.ajhg.2020.01.002 (Original work published 2020)