A novel mutation causing mild, atypical fumarylacetoacetase...

Orphanet Journal of Rare Diseases 2009 / 12 Vol. 4; Iss. 1

A novel mutation causing mild, atypical fumarylacetoacetase deficiency (Tyrosinemia type I): a case report

David Cassiman, Renate Zeevaert, Elisabeth Holme, Eli-Anne Kvittingen, Jaak Jaeken
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Volume:
4
Language:
english
DOI:
10.1186/1750-1172-4-28
Date:
December, 2009
File:
PDF, 1.36 MB
english, 2009
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