Genome-wide association study identifies novel susceptibility loci for KIT D816V positive mastocytosis
Galatà, Gabriella, García-Montero, Andrés C., Kristensen, Thomas, Dawoud, Ahmed A.Z., Muñoz-González, Javier I., Meggendorfer, Manja, Guglielmelli, Paola, Hoade, Yvette, Alvarez-Twose, Ivan, Gieger, Christian, Strauch, Konstantin, Ferrucci, Luigi, Tanaka, Toshiko, Bandinelli, Stefania, Schnurr, Theresia M., Haferlach, Torsten, Broesby-Olsen, Sigurd, Vestergaard, Hanne, Møller, Michael Boe, Bindslev-Jensen, Carsten, Vannucchi, Alessandro M., Orfao, Alberto, Radia, Deepti, Reiter, Andreas, Chase, Andrew J., Cross, Nicholas C.P., Tapper, William J.
Published in American journal of human genetics (04.02.2021)
Published in American journal of human genetics (04.02.2021)
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A homozygous missense variant in CHRM3 associated with familial urinary bladder disease
Beaman, Glenda M., Galatà, Gabriella, Teik, Keng W., Urquhart, Jill E., Aishah, Ali, O'Sullivan, James, Bhaskar, Sanjeev S., Wood, Katherine A., Thomas, Huw B., O'Keefe, Raymond T., Woolf, Adrian S., Stuart, Helen M., Newman, William G.
Published in Clinical genetics (01.12.2019)
Published in Clinical genetics (01.12.2019)
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