Two Japanese brothers with hereditary γ-glutamyl transpeptidase deficiency

Author： Iida M. Yasuhara T. Mochizuki H. Takakura H. Yanagisawa T. Kubo H.

ISSN： 0141-8955

Source： Journal of Inherited Metabolic Disease, Vol.28, Iss.1, 2005-01, pp. : 49-55

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Genetic Polymorphism of γ-Glutamyl Hydrolase in Chinese Acute Leukemia Children and Identification of a Novel Double Nonsynonymous Mutation

By Chen Xiaowen Wen Feiqiu Yue Lijie Li Changgang

Pediatric Hematology and Oncology, Vol. 29, Iss. 4, 2012-04 ,pp. : 303-312

Informa Healthcare

Access to resources Recommend Favorite

A Tale of Two Brothers: Anomalous Coronary Arteries in Two Siblings

By Devanagondi Rajiv Brenner Joel Vricella Luca Ravekes William

Pediatric Cardiology, Vol. 29, Iss. 4, 2008-07 ,pp. : 816-819

Springer Publishing Company

Access to resources Recommend Favorite

Differential response to interferon-γ therapy in a family with dominant negative partial interferon-γ receptor1 deficiency

By Smyth Anita Jackson Paul Lammas David Asghar M. Crockard Alistair Casanova Jean-Laurent Kumararatne Dinakantha Edgar J.

European Journal of Pediatrics, Vol. 165, Iss. 1, 2006-01 ,pp. : 71-72

Springer Publishing Company

Access to resources Recommend Favorite

Disappearance of congenital noncompaction in hereditary cobalamin-C-deficiency 2.5 years after birth

By Finsterer Josef Stöllberger Claudia

Journal of Inherited Metabolic Disease, Vol. 36, Iss. 6, 2013-11 ,pp. : 1083-1084

Springer Publishing Company

Access to resources Recommend Favorite

Intracerebral Mass Bleeding in a Term Neonate: Manifestation of Hereditary Protein S Deficiency with a New Mutation in the PROS1 Gene

Neonatology, Vol. 98, Iss. 4, 2010-05 ,pp. : 337-340

Karger

Access to resources Recommend Favorite