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Whittaker DE, Oleari R, Gregory LC, et al. A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia. J Clin Invest. 2021;131(24)doi: 10.1172/JCI141587.
Whittaker, D. E., Oleari, R., Gregory, L. C., Le Quesne-Stabej, P., Williams, H. J., Torpiano, J. G., Formosa, N., Cachia, M. J., Field, D., Lettieri, A., Ocaka, L. A., Paganoni, A. J., Rajabali, S. H., Riegman, K. L., De Martini, L. B., Chaya, T., Robinson, I. C., Furukawa, T., Cariboni, A., Basson, M. A., & Dattani, M. T. (2021). A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia. The Journal of clinical investigation, 131(24), . https://doi.org/10.1172/JCI141587
Whittaker, Danielle E, et al. "A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia." The Journal of clinical investigation vol. 131,24 (2021). doi: https://doi.org/10.1172/JCI141587
Whittaker DE, Oleari R, Gregory LC, Le Quesne-Stabej P, Williams HJ, Torpiano JG, Formosa N, Cachia MJ, Field D, Lettieri A, Ocaka LA, Paganoni AJ, Rajabali SH, Riegman KL, De Martini LB, Chaya T, Robinson IC, Furukawa T, Cariboni A, Basson MA, Dattani MT. A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia. J Clin Invest. 2021 Dec 15;131(24). doi: 10.1172/JCI141587. PMID: 34730112; PMCID: PMC8670848.
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