Metachromatic leukodystrophy (MLD), a lysosomal storage disease caused by the deficiency of arylsulfatase A (ASA), is inherited as an autosomal recessive trait, and its frequency is estimated to be 1 in 40,000 live births. Genomic DNA from 21 MLD patients (14 late-infantile and 7 juvenile cases) was
Analysis of the guinea-pig estrogen-regulated gec1/GABARAPL1 gene promoter and identification of a functional ERE in the first exon
✍ Scribed by Sandrine Vernier-Magnin; Christophe Nemos; Virginie Mansuy; Fabrice Tolle; Laure Guichard; Régis Delage-Mourroux; Michèle Jouvenot; Annick Fraichard
- Book ID
- 113485392
- Publisher
- Elsevier Science
- Year
- 2005
- Tongue
- English
- Weight
- 486 KB
- Volume
- 1731
- Category
- Article
- ISSN
- 0167-4781
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