Browsing by Author "Morgan, Neil"
Now showing 1 - 2 of 2
- Results Per Page
- Sort Options
Item The calcium-independent phospholipase A2 gene, PLA2G6, is mutated in a spectrum of childhood neurodegenerative disorders with high brain iron(Bmj Publishing Group, 2006-09) Morgan, Neil; Westaway, Shawn K.; Morton, Jenny; Gregory, Allison; Gissen, Paul; Sonek, S.; Coryell, Jessi L.; Canham, N.; Nardocci, Nardo; Zorzi, Giovanna; Pasha, Shanaz; Rodriguez, D.; Desguerre, Isabelle; Mubaidin, A.; Bertini, Enrico; Trembath, Richard C.; Simonati, A.; Schanen, Carolyn; Johnson, Colin A.; Levinson, B.; Woods, Christopherg; Wilmot, Brett; Kramer, P.; Gitschier, J.; Hayflick, Susan J.; Maher, E. R.; Cangül, H.; Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı.Item Locus heterogeneity and novel TSHR mutations in consanguineous families with congenital non-goitrous hypothyroidism(BMJ Publing Group, 2010-09) Cangül, Hakan; Aycan, Zehra; Morgan, Neil; Forman, Julia; Çetinkaya, Semra; Baş, Veysel; Demir, Korcan; Yuca, Sevil Arı; Kirby, Gail; Pasha, Shanaz; Kendall, Michaela; Hoegler, Wolfgang; Barret, T. G.; Maher, E. R.; Sağlam, Halil; Yakut, Tahsin; Gülten, Tuna; Karkucak, Mutlu; Eren, Erdal; Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı.; Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı.; 0000-0003-0710-5422; 0000-0002-1684-1053; C-7392-2019; AAM-1734-2020