Mutations in adar1, ifih1, and rnaseh2B presenting as spastic paraplegia.
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Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family with adar1 mutation.Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcifications.11.69, Save.Dev Med Child Neurol.PMC free article: PMC PubMed: Rice GI, Reijns MA, Coffin SR, Forte GM, Anderson BH, Szynkiewicz M, Gornall H, Gent D, Leitch A, Botella MP, Fazzi E, Gener B, appartement huren innsbruck Lagae L, Olivieri I, Orcesi S, Swoboda KJ, Perrino FW, Jackson AP, Crow.PubMed: 19012351, chitayat D, Meagher-Villemure K, Mamer OA, O'Gorman A, Hoar DI, Silver K, Scriver.PubMed: Desanges C, Lebon P, Bauman C, Vuillard E, Garel C, Cordesse was frauen wollen ofdb A, Oury JF, Crow Y, Luton.PubMed: Ramantani G, Kohlhase J, Hertzberg C, Innes AM, Engel K, Hunger S, Borozdin W, Mah JK, Ungerath K, Walkenhorst H, Richardt HH, Buckard J, Bevot A, Siegel C, von Stülpnagel C, Ikonomidou C, Thomas K, Proud V, Niemann F, Wieczorek D, Häusler M, Niggemann.Buy the Full Version, you're Reading a Free Preview, pages 250 to 397 are not shown in this preview.When caught, his father arranged for Huh Joon and his mother to leave for Kyung San more, this great historical drama about the stormy life story of Hur Jun, a legendary doctor of the Chosun Dynasty.
PMC free article: PMC PubMed: Rice G, Patrick T, Parmar R, Taylor CF, Aeby A, Aicardi J, Artuch R, Montalto SA, Bacino CA, Barroso B, Baxter P, Benko WS, Bergmann C, Bertini E, Biancheri R, Blair EM, Blau N, Bonthron DT, Briggs T, Brueton.A type I interferon signature identifies bilateral striatal necrosis due to mutations in adar1.PMC free article: PMC PubMed: Rice GI, del Toro Duany Y, Jenkinson EM, Forte GM, Anderson BH, Ariaudo G, Bader-Meunier B, Baildam EM, Battini R, Beresford MW, Casarano M, Chouchane M, Cimaz R, Collins AE, Cordeiro NJ, Dale RC, Davidson JE, De Waele L, Desguerre.PubMed: Lee-Kirsch MA, Chowdhury D, Harvey S, Gong M, Senenko L, Engel K, Pfeiffer C, Hollis T, Gahr M, Perrino FW, Lieberman J, Hubner.PubMed: Reardon W, Hockey A, Silberstein P, Kendall B, Farag TI, Swash M, Stevenson R, Baraitser.Prenatal diagnosis of Aicardi-Goutieres syndrome.Aicardi-Goutieres syndrome: an update and results of interferon-alpha studies.PubMed: 12365358, blau N, Bonafe L, Krageloh-Mann I, Thony B, Kierat L, Hausler M, Ramaekers.




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