Inherited lysosomal storage disease associated with deficiencies of β-galactosidase and α-neuraminidase in sheep-Reference-Cited by-同舟云学术

Inherited lysosomal storage disease associated with deficiencies of β-galactosidase and α-neuraminidase in sheep

Published:1988-09 Issue:1 Volume:31 Page:39-56
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Ahern-Rindell Amelia J.,Prieur David J.,Murnane Robert D.,Raghavan Srinivasa S.,Daniel Peter F.,McCluer Robert H.,Walkley Steven U.,Parish Steven M.,Opitz John M.,Reynolds James F.

Publisher

Wiley

Subject

Genetics(clinical)

Reference50 articles.

1. Methods for the quantitative estimation of N-acetylneuraminic acid and their application to hydrolysates of sialomucoids

2. Atypical expression of ß-galactosidase deficiency in a child with Hurler-like features but without neurological abnormalities

3. Neuronal GM 1 Gangliosidosis in a Siamese Cat with β-Galactosidase Deficiency

4. GM1 gangliosidosis (type 1) in a cat

5. GM1 gangliosidosis in a cat

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