Beta-mannosidosis
| Beta-mannosidosis | |
| OMIM | 248510 |
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| DiseasesDB | 34529 |
| MeSH | D044905 |
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Beta-mannosidosis, also called lysosomal beta-mannosidase deficiency,[1] is a rare autosomal recessive[2] form of mannosidosis associated with MANBA.[3]
References
- ↑ Online Mendelian Inheritance in Man (OMIM) 248510
- ↑ Kleijer, Wj; Hu, P; Thoomes, R; Boer, M; Huijmans, Jg; Blom, W; Van, Diggelen, Op; Seemanova, E; Macek, M (1990). "Beta-mannosidase deficiency: heterogeneous manifestation in the first female patient and her brother". Journal of inherited metabolic disease. 13 (6): 867–72. doi:10.1007/BF01800211. ISSN 0141-8955. PMID 2079835.
- ↑ Uchino, Y; Fukushige, T; Yotsumoto, S; Hashiguchi, T; Taguchi, H; Suzuki, N; Konohana, I; Kanzaki, T (2003). "Morphological and biochemical studies of human beta-mannosidosis: identification of a novel beta-mannosidase gene mutation". The British journal of dermatology. 149 (1): 23–9. doi:10.1046/j.1365-2133.2003.05365.x. ISSN 0007-0963. PMID 12890191. Unknown parameter
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