Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Samantha S. Davis"'
Autor:
Tyler B. Johnson, Jon J. Brudvig, Shibi Likhite, Melissa A. Pratt, Katherine A. White, Jacob T. Cain, Clarissa D. Booth, Derek J. Timm, Samantha S. Davis, Brandon Meyerink, Ricardo Pineda, Cassandra Dennys-Rivers, Brian K. Kaspar, Kathrin Meyer, Jill M. Weimer
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
CLN3 disease, caused by biallelic mutations in the CLN3 gene, is a rare pediatric neurodegenerative disease that has no cure or disease modifying treatment. The development of effective treatments has been hindered by a lack of etiological knowledge,
Externí odkaz:
https://doaj.org/article/cb379df157064165b746745383d34428
Autor:
McKayla J. Poppens, Jacob T. Cain, Tyler B. Johnson, Katherine A. White, Samantha S. Davis, Rachel Laufmann, Alexander D. Kloth, Jill M. Weimer
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
Abstract Background CLN6-Batten disease is a rare neurodevelopmental disorder characterized pathologically by the accumulation of lysosomal storage material, glial activation and neurodegeneration, and phenotypically by loss of vision, motor coordina
Externí odkaz:
https://doaj.org/article/7b28cbfe339a47748e8ffc5fdc88fd71
Autor:
Poppens, McKayla J.1 Mckayla.Poppens@sanfordhealth.org, Cain, Jacob T.1 Jacob.Cain@sanfordhealth.org, Johnson, Tyler B.1 Tyler.Johnson2@sanfordhealth.org, White, Katherine A.1 Katherine.White@sanfordhealth.org, Davis, Samantha S.1 Samantha.Davis2@sanfordhealth.org, Laufmann, Rachel1 Rachel.Laufmann2@sanfordhealth.org, Kloth, Alexander D.2 akloth@augie.edu, Weimer, Jill M.1,3 Jill.Weimer@sanfordhealth.org
Publikováno v:
Orphanet Journal of Rare Diseases. 1/21/2019, Vol. 14 Issue 1, pN.PAG-N.PAG. 1p.
Publikováno v:
Gene Therapy Weekly; 4/13/2023, p1036-1036, 1p