The principles of human biochemical genetics / Harry Harris.

  • Harry Harris
Date:
1975
Catalogue details

Licence: Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)

Credit: The principles of human biochemical genetics / Harry Harris. Source: Wellcome Collection.

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    Siíhjecf index Steroid 21-hydroxylase deficiency, 393 Storage diseases glycogen fîtorage diseases, 210-216 lysosomal storage diseases, 216-232, 374-376 Subunit structures of enzymes, 34-37, 84-90 Sucrose and isomaltose intolerance, 373 Sulphite oxidase, 384 Sulphoiduronate sulphatase. 177-178, 221, 374 Superoxide dismutase, 74, 88, 89, 303 Suxamethonium sensitivity, 150ff, 386 Tay-Sachs disease, 218, 222, 223, 227-230, 237, 313, 331, 374 Thaiassaemias, 133-146, 289 a-thalassaemia, 142-146 /?-thalassaemia, 134-138 d/3-thalassaemia (F-thalassaemia), MO¬ KI Thalassaemia major, 134-135 Thaiassaemia minor, 135 Transferrin, 281, 398 Transport defects, see Aminoacid transport Trióse phosphate isomerase, 236, 303, 355, 370 ai-Trypsin inhibitor (serum), 360-362, 365, 399 Trypsinogen, 389 Tyrosine aminotransferase. 383 Tyrosinosis, 330 Unequal crossing-over, 99, 103-112 Urea disorders of urea cycle, 204-210 biosynthesis of, 205-206 Uridine monophosphate kinase, 39o Urocanase, 378 Urocanic aciduria, 378 Uroporphyrinogen III cosynthetase, 240, 391 Uroporphyrinogen synthetase, 240-241.391 Valine transaminase, 381 Vitamin-D dependent rickets, 391 Von Gierke's disease, 213, 215, 237, 371 Wolman's disease, 219, 232, 376 Xanthine oxidase, 384 Xanthinuria, 384 Xanthurenic aciduria, 383 Xm (serum «2 macroglobulin) poly¬ morphism, 399 L-xylulose reductase deficiency, 371 Xylulosuria (xyloketosuria), see Pentosuria