TY  - BOOK
AU  - Scriver, C.R. (ed)
AU  - Beaudet, A.L. (ed)
AU  - Sly, W.S. (ed)
AU  - Valle, D. (ed)
TI  - The metabolic and molecular bases of inherited disease volume II
SN  - 0071363203
PY  - 2001///
CY  - New York
PB  - McGraw-Hill
KW  - GENETIC DISEASES, INBORN
KW  - METABOLIC DISEASES
KW  - METABOLISM, INBORN ERRORS
N1  - Amino acids; organic acids; disorders of mitochondrial function; purines and pyrimidines; lipids; porphyrins; metals; peroxisomes
N2  - Hardback; This is a reference guide for information in the field of molecular biology. It covers areas such as, the effects of genes, their location on the chromosomes and what treatment, if any, can be recommended to paediatricians and other clinicians whose patients show certain signs and symptoms. This eighth edition has been expanded and updated to include colon cancer, breast cancer, triplet repeat disorders, fragile X mental retardation, biochemical and molecular mechanisms, and clinical diagnosis and management approaches
ER  -