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2014, Número 2

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Ann Hepatol 2014; 13 (2)


Tyrosinemia type I: clinical and biochemical analysis of patients in Mexico

Fernández-Lainez C, Ibarra-González I, Belmont-Martínez L, Monroy-Santoyo S, Guillén-López S, Vela-Amieva M

Idioma: Ingles.
Referencias bibliográficas: 34
Paginas: 265-272
Archivo PDF: 195.93 Kb.


RESUMEN

Sin resumen.


REFERENCIAS (EN ESTE ARTÍCULO)

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  2. Held PK. Disorders of tyrosine catabolism. Mol Genet Metab 2006; 88: 103-6.

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  6. Mak CM, Lam CW, Chim S, Siu TS, Ng KF, Tam S. Biochemical and molecular diagnosis of tyrosinemia type I with two novel FAH mutations in a Hong Kong chinese patient: recommendation for expanded newborn screening in Hong Kong. Clin Biochem 2013; 46: 155-9.

  7. Bartlett DC, Preece MA, Holme E, Lloyd C, Newsome PN, McKiernan PJ. Plasma succinylacetone is persistently raised after liver transplantation in tyrosinaemia type 1. J Inherit Metab Dis 2013; 36: 15-20.

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