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Vidali S, Gerlini R, Thompson K, et al. Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypes. EMBO Mol Med. 2021;13(12):e14397doi: 10.15252/emmm.202114397.
Vidali, S., Gerlini, R., Thompson, K., Urquhart, J. E., Meisterknecht, J., Aguilar-Pimentel, J. A., Amarie, O. V., Becker, L., Breen, C., Calzada-Wack, J., Chhabra, N. F., Cho, Y. L., da Silva-Buttkus, P., Feichtinger, R. G., Gampe, K., Garrett, L., Hoefig, K. P., Hölter, S. M., Jameson, E., Klein-Rodewald, T., Leuchtenberger, S., Marschall, S., Mayer-Kuckuk, P., Miller, G., Oestereicher, M. A., Pfannes, K., Rathkolb, B., Rozman, J., Sanders, C., Spielmann, N., Stoeger, C., Szibor, M., Treise, I., Walter, J. H., Wurst, W., Mayr, J. A., Fuchs, H., Gärtner, U., Wittig, I., Taylor, R. W., Newman, W. G., Prokisch, H., Gailus-Durner, V., & Hrabě de Angelis, M. (2021). Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypes. EMBO molecular medicine, 13(12), e14397. https://doi.org/10.15252/emmm.202114397
Vidali, Silvia, et al. "Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypes." EMBO molecular medicine vol. 13,12 (2021): e14397. doi: https://doi.org/10.15252/emmm.202114397
Vidali S, Gerlini R, Thompson K, Urquhart JE, Meisterknecht J, Aguilar-Pimentel JA, Amarie OV, Becker L, Breen C, Calzada-Wack J, Chhabra NF, Cho YL, da Silva-Buttkus P, Feichtinger RG, Gampe K, Garrett L, Hoefig KP, Hölter SM, Jameson E, Klein-Rodewald T, Leuchtenberger S, Marschall S, Mayer-Kuckuk P, Miller G, Oestereicher MA, Pfannes K, Rathkolb B, Rozman J, Sanders C, Spielmann N, Stoeger C, Szibor M, Treise I, Walter JH, Wurst W, Mayr JA, Fuchs H, Gärtner U, Wittig I, Taylor RW, Newman WG, Prokisch H, Gailus-Durner V, Hrabě de Angelis M. Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypes. EMBO Mol Med. 2021 Dec 07;13(12):e14397. doi: 10.15252/emmm.202114397. Epub 2021 Nov 08. PMID: 34750991; PMCID: PMC8649870.
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