GM1-gangliosidosis is a lysosomal storage disorder caused by a deficiency of beta-galactosidase. It is mainly characterized by progressive neurodegeneration and in its most severe infantile form it leads to death before the age of four. We have performed molecular analysis of five patients with the
โฆ LIBER โฆ
Infantile generalized GM1 gangliosidosis: High incidence in the Maltese Islands
โ Scribed by H.M. Lenicker; P. Vassallo Agius; E.P. Young; S.P. Attard Montalto
- Book ID
- 110222562
- Publisher
- Springer
- Year
- 1997
- Tongue
- English
- Weight
- 6 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0141-8955
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