Rickettsia felis DNA recovered from a child who lived in southern Africa 2000 years ago.
Communications Biology
Rifkin, Riaan F RF; Vikram, Surendra S; Alcorta, Jaime J; Ramond, Jean-Baptiste JB; Cowan, Don A DA; Jakobsson, Mattias M; Schlebusch, Carina M CM; Lombard, Marlize M
Two Approaches for a Genetic Analysis of Pompe Disease: A Literature Review of Patients with Pompe Disease and Analysis Based on Genomic Data from the General Population.
Children (Basel, Switzerland)
Park, Kyung-Sun KS
Publication Date: 2021-07-16
Variant appearance in text: GAA: 2297A>G; Tyr766Cys
Structure of PDE3A-SLFN12 complex reveals requirements for activation of SLFN12 RNase.
Nature Communications
Garvie, Colin W CW; Wu, Xiaoyun X; Papanastasiou, Malvina M; Lee, Sooncheol S; Fuller, James J; Schnitzler, Gavin R GR; Horner, Steven W SW; Baker, Andrew A; Zhang, Terry T; Mullahoo, James P JP; Westlake, Lindsay L; Hoyt, Stephanie H SH; Toetzl, Marcus M; Ranaghan, Matthew J MJ; de Waal, Luc L; McGaunn, Joseph J; Kaplan, Bethany B; Piccioni, Federica F; Yang, Xiaoping X; Lange, Martin M; Tersteegen, Adrian A; Raymond, Donald D; Lewis, Timothy A TA; Carr, Steven A SA; Cherniack, Andrew D AD; Lemke, Christopher T CT; Meyerson, Matthew M; Greulich, Heidi H
Newborn Screening for Pompe Disease in Illinois: Experience with 684,290 Infants.
International Journal Of Neonatal Screening
Burton, Barbara K BK; Charrow, Joel J; Hoganson, George E GE; Fleischer, Julie J; Grange, Dorothy K DK; Braddock, Stephen R SR; Hitchins, Lauren L; Hickey, Rachel R; Christensen, Katherine M KM; Groepper, Daniel D; Shryock, Heather H; Smith, Pamela P; Shao, Rong R; Basheeruddin, Khaja K
GAA variants and phenotypes among 1,079 patients with Pompe disease: Data from the Pompe Registry.
Human Mutation
Reuser, Arnold J J AJJ; van der Ploeg, Ans T AT; Chien, Yin-Hsiu YH; Llerena, Juan J; Abbott, Mary-Alice MA; Clemens, Paula R PR; Kimonis, Virginia E VE; Leslie, Nancy N; Maruti, Sonia S SS; Sanson, Bernd-Jan BJ; Araujo, Roberto R; Periquet, Magali M; Toscano, Antonio A; Kishnani, Priya S PS; On Behalf Of The Pompe Registry Sites,
Publication Date: 2019-11
Variant appearance in text: GAA: 2297A>G; Tyr766Cys
A cross-sectional single-centre study on the spectrum of Pompe disease, German patients: molecular analysis of the GAA gene, manifestation and genotype-phenotype correlations.
Orphanet Journal Of Rare Diseases
Herzog, Andreas A; Hartung, Ralf R; Reuser, Arnold J J AJ; Hermanns, Pia P; Runz, Heiko H; Karabul, Nesrin N; Gökce, Seyfullah S; Pohlenz, Joachim J; Kampmann, Christoph C; Lampe, Christina C; Beck, Michael M; Mengel, Eugen E