Peroxisomal and Mitochondrial Defects in the Cerebro-Hepato-Renal Syndrome
Author:
Affiliation:
1. Departments of Pathology, Neurology, and Pediatrics, and Rose F. Kennedy Center for Research in Mental Retardation and Human Development, Albert Einstein College of Medicine, Bronx, New York 10461
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference34 articles.
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3. BOWEN, P, FAMILIAL SYNDROME OF MULTIPLE CONGENITAL DEFECTS, BULLETIN OF THE JOHNS HOPKINS HOSPITAL 114: 402 (1964).
4. BURSTONE, M.S., MODIFICATIONS OF HISTOCHEMICAL TECHNIQUES FOR DEMONSTRATION OF CYTOCHROME OXIDASE, JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY 9: 59 (1961).
5. CITKOWITZ, E, PEROXISOMES IN DORSAL ROOT GANGLIA, JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY 21: 34 (1973).
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