Juvenile GM2 gangliosidosis: Partial deficiency of bexosaminidase A-Reference-Cited by-同舟云学术

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Juvenile GM2 gangliosidosis: Partial deficiency of bexosaminidase A

Published:1970-12 Issue:6 Volume:77 Page:1063-1065
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Okada Shintaro,Veath M. Lois,O'Brien John S.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference7 articles.

1. Über das Verhalten der Ganglioside im Gehirn bei 2 Fällen von spätinfantiler amaurotischer Idiotie;Bernheimer;Wein. Klin. Wschr.,1968

2. G5-ganglioside variant of systemic late infantile lipidosis;Volk;Arch. Path.,1969

3. Juvenile GM2 gangliosidosis: Clinical variant of Tay-Sachs disease or a new disease;Suzuki;Neurology,1970

4. Tay-Sachs disease: Generalized absence of a β-D-N-acetylhexosaminidase component;Okada;Science,1969

5. Menkes, J., Okada, S., O'Brien, J. S., Grippo,J., Andrews, J. M., and Cancilla, P. A.: In preparation.

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