A new Caucasian case of neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD): A clinical, molecular, and functional study-Reference-Cited by-同舟云学术

A new Caucasian case of neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD): A clinical, molecular, and functional study

Published:2011-12 Issue:4 Volume:104 Page:501-506
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Fiermonte Giuseppe,Parisi Giovanni,Martinelli Diego,De Leonardis Francesco,Torre Giuliano,Pierri Ciro Leonardo,Saccari Alessia,Lasorsa Francesco Massimo,Vozza Angelo,Palmieri Ferdinando,Dionisi-Vici Carlo

Funder

MIUR

Center of Excellence in Genomics (CEGBA)

Fondazione Cassa di Risparmio di Puglia, Biotecnoter project (The Apulia Region)

Italian Human ProteomeNet

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference38 articles.

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3. Diseases caused by defects of mitochondrial carriers: a review;Palmieri;Biochim. Biophys. Acta,2008

4. Neonatal presentation of adult-onset type II citrullinemia;Ohura;Hum. Genet.,2001

5. Citrin deficiency, a perplexing global disorder;Dimmock;Mol. Genet. Metab.,2009

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