1 (derived from normal marrow) in feline alpha-mannosidosis.

2 cal or pathological progression of the alpha-mannosidosis.

3 cDNA isolated from a goat affected with beta-mannosidosis.

4 r injections in the cat model of human alpha-mannosidosis.

5    Deficiency of this enzyme results in beta-mannosidosis, a lysosomal storage disease characterized

6 his mouse model closely resembles human beta-mannosidosis and provides a useful tool for studying the

7 and that obligate carriers in a caprine beta-mannosidosis colony were heterozygous.

8  two siblings differently affected with beta-mannosidosis demonstrated a homozygous A-->G transition

9 arides, oligosaccharides isolated from alpha-mannosidosis fibroblasts, and p-nitrophenyl-alpha-D-mann

10 in all human tissues tested, including alpha-mannosidosis fibroblasts, while minor transcripts of 3.6

11 utation that is associated with caprine beta-mannosidosis has been identified.

12                                   Human beta-mannosidosis is an autosomal recessive, lysosomal storag

13 ation among the reported cases of human beta-mannosidosis is variable, even among members of the same

14 erism in a goat with an atypically mild beta-mannosidosis phenotype.

15                                In human beta-mannosidosis, the clinical presentation is variable and

16 n, confirmed that animals affected with beta-mannosidosis were homozygous for the mutation and that o