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2009, Number SA

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Bioquimia 2009; 34 (SA)

Detección de glucogenosis en población mexicana. Descripción del fenotipo clínico y bioquimico

Ramírez GSA, Pérez GG, Ornelas AML, Ruíz MR, Flores ALJ
Full text How to cite this article

Language: Spanish
References: 4
Page: 113
PDF size: 118.23 Kb.


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REFERENCES

  1. Coleman RA, Winter HS, Wolf B, et al. Glycogen debranching enzyme deficiency: long-term study of serum enzyme activities and clinical features. J Inherit Metab Dis. 1992; 15 (6):869-81

  2. Meza-Azael A, Ayub M, Cantu JM, Flores LJ. Diet therapy in severe clinical expresión of debrancher deficiency. Arch. Invest.Med. 1991; 22: 285.

  3. Flores LJ, Gasca-Centeno E and Grier RE. Hepatic phosphorylase b kinase deficiency with normal enzyme activity in leucocytes. Journal of Pediatrics 1988; 113(5); 865-867.

  4. Sotelo N, García R, Tostado R, Dhanakotti N. Fanconi– Bickel Síndrome. Ann Hepatol 2008; 7(2): 163-167.




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Bioquimia. 2009;34