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A presentation of clinical, genetic, neuropathological, enzymatic, and neurochemical developments in storage disease research. Using the multidisciplinary approach, it covers ganglioside diseases and theoretical effects of enzyme deficiencies. There are seven chapters, each written by an authority in the field and an extensive appendix giving newer methods useful in the study of these complicated lipids. Each chapter concludes with a complete bibliography including titles, and there is a subject index for the entire work. A book of interest to students of human genetics and diseases of lipid metabolism.
The Gangliosidoses.. Ann Intern Med. ;86:124. doi: 10.7326/0003-4819-86-1-124_5
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Published: Ann Intern Med. 1977;86(1):124.
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Print ISSN: 0003-4819 | Online ISSN: 1539-3704
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