Mutations in the gene encoding the neuronal cell adhesion molecule L1 are responsible for several syndromes with clinical overlap, including X-linked hydrocephalus (XLH, HSAS), MASA (mental retardation, aphasia, shuffling gait, adducted thumbs) syndrome, complicated X-linked spastic paraplegia (SP l
โฆ LIBER โฆ
The human neural cell adhesion molecule L1 functions as a costimulatory molecule in T cell activation
โ Scribed by Larissa B. Balaian; Thomas Moehler; Anthony M. P. Montgomery
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 113 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0014-2980
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