Clinical and genetic characteristics of type I sialidosis patients in mainland China

OBJECTIVE: Type I sialidosis (ST‐1) is a rare autosomal recessive inherited disorder. To date, there has been no study on ST‐1 patients in mainland China. METHODS: We reported in detail the cases of five Chinese ST‐1 patients from two centers, and summarized all worldwide cases. Then, we compared th...

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Detalles Bibliográficos
Autores principales: Lv, Rui‐Juan, Li, Tao‐Ran, Zhang, Yu‐Di, Shao, Xiao‐Qiu, Wang, Qun, Jin, Li‐Ri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318099/
https://www.ncbi.nlm.nih.gov/pubmed/32472645
http://dx.doi.org/10.1002/acn3.51058

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318099/
https://www.ncbi.nlm.nih.gov/pubmed/32472645
http://dx.doi.org/10.1002/acn3.51058

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