Mitochondrial Myopathy and Congenital Cataract
The autosomal recessive syndrome characterized by mitochondrial myopathy of cardiac and skeletal muscle, congenital cataract and lactic acidosis is described in two forms following a retrospective study of 16 patients at the University of Nijmegen, The Netherlands.
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| Main Author: | |
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| Format: | Book |
| Published: |
Pediatric Neurology Briefs Publishers,
1993-05-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |