Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Ling-Han Ma"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-9 (2024)
Abstract Background Sialidosis type 1 (ST-1) is a rare autosomal recessive disorder caused by mutation in the NEU1 gene. However, limited reports on ST-1 patients in the Chinese mainland are available. Methods This study reported the genetic and clin
Externí odkaz:
https://doaj.org/article/77d2637d03f34ebca0c81b0edbb3ac14