A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance
- 1 January 1976
- journal article
- case report
- Published by Elsevier in The American Journal of Medicine
- Vol. 60 (1) , 23-32
- https://doi.org/10.1016/0002-9343(76)90529-5
Abstract
No abstract availableKeywords
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