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pro vyhledávání: '"Katharina Janik"'
Autor:
Jessica Schäfer, Nicole Wenck, Katharina Janik, Joshua Linnert, Katarina Stingl, Susanne Kohl, Kerstin Nagel-Wolfrum, Uwe Wolfrum
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 11 (2023)
Human Usher syndrome (USH) is the most common form of hereditary combined deaf-blindness. USH is a complex genetic disorder, and the pathomechanisms underlying the disease are far from being understood, especially in the eye and retina. The USH1C gen
Externí odkaz:
https://doaj.org/article/c34b9e213e084b9ca8c16ed06537e22a
