APA (7th ed.) Citation

M, S., NCP, L., TN, U. L., Y, Z., Y, W., M, S., . . . LN, N. (2026). A hypomorphic FLVCR2 variant resulting in moderate transport deficiency causes hydranencephaly syndrome with brain calcifications. European journal of human genetics : EJHG, 34(3), 324. https://doi.org/10.1038/s41431-025-01836-7

Chicago Style (17th ed.) Citation

M, Scala, et al. "A Hypomorphic FLVCR2 Variant Resulting in Moderate Transport Deficiency Causes Hydranencephaly Syndrome with Brain Calcifications." European Journal of Human Genetics : EJHG 34, no. 3 (2026): 324. https://doi.org/10.1038/s41431-025-01836-7.

MLA (9th ed.) Citation

M, Scala, et al. "A Hypomorphic FLVCR2 Variant Resulting in Moderate Transport Deficiency Causes Hydranencephaly Syndrome with Brain Calcifications." European Journal of Human Genetics : EJHG, vol. 34, no. 3, 2026, p. 324, https://doi.org/10.1038/s41431-025-01836-7.