Add to ORKGMucopolysaccharidosis type VI (MPS VI) is a lysosomal storage disease caused by a deficiency of
The mucopolysaccharidoses are a group of lysosomal storage diseases caused by deficiency of an enzym...
The release of new DNA-based diagnostic tools has increased tremendously in companion animals. Over ...
Mucolipidosis II (ML II), also called I-cell disease, is a unique lysosomal storage disease caused b...
Mucopolysaccharidosis type VI (MPS VI) is a lysosomal storage disease caused by a deficiency of N-ac...
Mucopolysaccharidosis type VI (MPS VI) is an autosomal recessive disease caused by a deficiency of N...
Mucopolysaccharidosis type VI (MPS VI), a lysosomal storage disease, is one of the more prevalent in...
The missense mutation, L476P, in the N-acetylgalactosamine 4-sulfatase (4S) gene, has previously bee...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Abstract. A male cat 12-1 4 weeks old had walking difficulties and an enlarged abdomen. Facial dysmo...
Abstract. Mucopolysaccharidosis VII was diagnosed in a domestic shorthair cat from California. The c...
Abstract Background Mucolipidosis II (ML II; I-cell disease) is caused by a deficiency of N-acetylgl...
Three cats with feline arylsulfatase-B-deficient mucopolysaccharidosis were studied by light and tra...
Mucolipidosis II (ML II), also called I-cell disease, is a unique lysosomal storage disease caused b...
The mucopolysaccharidoses are a group of lysosomal storage diseases caused by deficiency of an enzym...
The release of new DNA-based diagnostic tools has increased tremendously in companion animals. Over ...
Mucolipidosis II (ML II), also called I-cell disease, is a unique lysosomal storage disease caused b...
Mucopolysaccharidosis type VI (MPS VI) is a lysosomal storage disease caused by a deficiency of N-ac...
Mucopolysaccharidosis type VI (MPS VI) is an autosomal recessive disease caused by a deficiency of N...
Mucopolysaccharidosis type VI (MPS VI), a lysosomal storage disease, is one of the more prevalent in...
The missense mutation, L476P, in the N-acetylgalactosamine 4-sulfatase (4S) gene, has previously bee...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Abstract. A male cat 12-1 4 weeks old had walking difficulties and an enlarged abdomen. Facial dysmo...
Abstract. Mucopolysaccharidosis VII was diagnosed in a domestic shorthair cat from California. The c...
Abstract Background Mucolipidosis II (ML II; I-cell disease) is caused by a deficiency of N-acetylgl...
Three cats with feline arylsulfatase-B-deficient mucopolysaccharidosis were studied by light and tra...
Mucolipidosis II (ML II), also called I-cell disease, is a unique lysosomal storage disease caused b...
The mucopolysaccharidoses are a group of lysosomal storage diseases caused by deficiency of an enzym...
The release of new DNA-based diagnostic tools has increased tremendously in companion animals. Over ...
Mucolipidosis II (ML II), also called I-cell disease, is a unique lysosomal storage disease caused b...