Tyrosinemia Type II with Incomplete Richner-Hanhart's Syndrome
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-4362.1988.tb02336.x/fullpdf
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1. Neue Sonderformen von Keratosis palmo-plantaris, u. a. eine regelmäßig-dominante mit systematisierten Lipomen, ferner 2 einfach-rezessive mit Schwachsinn und z.T. mit Hornhautveränderungen des Auges (Ektodermalsyndrom)
2. Tyrosinemia II. A large North Carolina kindred
3. Soluble and mitochondrial forms of tyrosine aminotransferase. Relation to human tyrosinemia
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2. Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: Identification and structural characterization of two novel TAT mutations;Molecular Genetics and Metabolism;2006-06
3. Plantar keratoderma: a manifestation of tyrosinemia type II (Richner-Hanhart Syndrome);Annals of Saudi Medicine;2005-09
4. Tyrosinemia Type II: Report of the First Four Cases in Saudi Arabia;Annals of Saudi Medicine;1998-09
5. Tyrosinemia II: Report of an Incomplete Case and Studies on the Hyperkeratotic Stratum corneum;Dermatology;1991
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