The metabolic basis of inherited disease I 6 edition. 1989.Brusilow, S.W. and Horwich, A.L. (1989) in The Metabolic Basis of Inherited Disease, 6th Edition (C.R. Scriver, A.L. Beaudet, W.S. Sly and D. Valle, eds.), pp. 629–670, McGraw-Hill, New York, NY....
The Metabolic Basis of Inherited Disease. McGraw-Hill: New York, 1992:2083–2103. Google Scholar Mock DM, Baswell DL, Baker H, Holman RT, Sweetman L . Biotin deficiency complicating parenteral alimentation: diagnosis, metabolic repercussions, and treatment. Ann NY Acad Sci 1985;447:314–334...
The metabolic and molecular bases of inherited disease: Vols I, II and III (7th edn) Glycogen is used as an almost universal energy store in animal tissues; its complex molecular structure requires the interaction of many biosynthetic and degradative enzymes, whose action is finely coordinated and...
, The Metabolic Basis of Inherited Disease (ed 5), McGraw-Hill, New York, NY (1983), p. 1654 Google Scholar 18 Prchal JT, Borgese N, Moore MR, Moreno H, Hegesh E, Hall MK Congenital methemoglobinemia due to methemoglobin reductase deficiency in two unrelated American black families Am...
The Metabolic and Molecular Bases of Inherited Disease. Edited by: Scriver CR, Beaudet AL, Sly WS, Valle D, Vogelstein B, Childs B, Kinzler KW. New York , McGraw-Hill; 2005. Online. http://genetics.accessmedicine.com. Google Scholar Sierra-Rivera E, Summar ML, Dasouki M, ...
The metabolic and molecular bases of inherited disease. Edited by: Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kinzler KW, Vogelstein B. McGraw-Hill, New York, 2005, 8: 2297-2326. Google Scholar Gregersen N, Andresen BS, Pedersen CB, Olsen RK, Corydon TJ, Bross P: ...
, Metabolic Basis of Inherited Disease, McGraw-Hill, New York (1989) 2751–2777.pp Google Scholar Beglova et al. 2002 N. Beglova, S.C. Blacklow, J. Takagi, T.A. Springer Cysteine-rich module structure reveals a fulcrum for integrin rearrangement upon activation Nat. Struct. Biol., 9 ...
Metabolic changes in the basal ganglia of patients with Huntington's disease: an in situ hybridization study of cytochrome oxidase subunit I mRNA (2002) Metabolic changes in the basal ganglia of patients with Huntington's disease: An in situ hybridization study of cytochrome oxidase subunit I mRNA...
S. Fredrickson: The Metabolic Basis of Inherited Disease. 4th Ed. pp. 1683-1710 (McGraw-Hill. New York. 1978). 14. Pallavrcini. J. C., Gabriel. 0 . . di Sanl'Agnese. P. A,. and Burkirk, E. R.: Isolation and characterization of carbohydrate-protein complexes from human sweat. ...
In: Scriver CR et al (eds) The metabolic and molecular bases of inherited disease. McGraw-Hill, New York, pp 4117–4146 Google Scholar Imperato-McGinley J, Guerrero L, Gautier T, Peterson RE (1974) Steroid 5α-reductase deficiency in man: an inherited form of male pseudohermaphroditism....