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Genetic analysis of a novel SUMF1 variation associated with a late infantile form of multiple sulfatase deficiency
BACKGROUND: Multiple sulfatase deficiency (MSD) (MIM#272200) is an ultra‐rare autosomal recessive lysosomal storage disorder caused by mutation of the Sulfatase Modifying Factor 1 (SUMF1) gene. METHODS: Herein, we report an eight‐year‐old boy with a late infantile form of multiple sulfatase deficien...
Autores principales: | Zhang, Jingjing, Ma, Dingyuan, Liu, Gang, Zeng, Huasha, Wang, Yuguo, Luo, Chunyu, Hu, Ping, Xu, Zhengfeng |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9756991/ https://www.ncbi.nlm.nih.gov/pubmed/36441600 http://dx.doi.org/10.1002/jcla.24786 |
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