Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Andres F. Pacheco Pacheco"'
Autor:
Jennifer J. Lee, Swetha Ramadesikan, Adrianna F. Black, Charles Christoffer, Andres F. Pacheco Pacheco, Sneha Subramanian, Claudia B. Hanna, Gillian Barth, Cynthia V. Stauffacher, Daisuke Kihara, Ruben Claudio Aguilar
Publikováno v:
Biomolecules, Vol 13, Iss 4, p 615 (2023)
Lowe Syndrome (LS) is a condition due to mutations in the OCRL1 gene, characterized by congenital cataracts, intellectual disability, and kidney malfunction. Unfortunately, patients succumb to renal failure after adolescence. This study is centered i
Externí odkaz:
https://doaj.org/article/f73ecfff1eae43f69d7628ffdc0d6114
Autor:
Lee, Jennifer J.1,2 (AUTHOR) lee3100@purdue.edu, Ramadesikan, Swetha1,2 (AUTHOR) black173@purdue.edu, Black, Adrianna F.1,2 (AUTHOR) apachecop@unal.edu.co, Christoffer, Charles3 (AUTHOR) christ35@purdue.edu, Pacheco, Andres F. Pacheco1,2 (AUTHOR) subram64@purdue.edu, Subramanian, Sneha1,2 (AUTHOR) clauh1@purdue.edu, Hanna, Claudia B.1,2 (AUTHOR) barthg@purdue.edu, Barth, Gillian1,2 (AUTHOR) cstauffa@purdue.edu, Stauffacher, Cynthia V.1,2 (AUTHOR) dkihara@purdue.edu, Kihara, Daisuke1,2,3 (AUTHOR), Aguilar, Ruben Claudio1,2 (AUTHOR) claudio@purdue.edu
Publikováno v:
Biomolecules (2218-273X). Apr2023, Vol. 13 Issue 4, p615. 18p.