A DISEASE, PROBABLY HEREDITARY, CHARACTERISED BY SEVERE MENTAL DEFICIENCY AND A CONSTANT GROSS ABNORMALITY OF AMINOACID METABOLISM
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference15 articles.
1. HEREDITARY PELLAGRA-LIKE SKIN RASH WITH TEMPORARY CEREBELLAR ATAXIA, CONSTANT RENAL AMINO-ACIDURIA, AND OTHER BIZARRE BIOCHEMICAL FEATURES
2. Wilson's disease
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4. HEREDITARY FORMS OF RICKETS AND OSTEOMALACIA
5. AMINO-ACID METABOLISM
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