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Two Italian patients with novel AAAS gene mutation expand allelic and phenotypic spectrum of triple A (Allgrove) syndrome

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Bibliographic Details
Published in:	Clinical genetics 2010-03, Vol.77 (3), p.298-301
Main Authors:	Palka, C, Giuliani, R, Brancati, F, Mohn, A, Di Muzio, A, Calabrese, O, Huebner, A, De Grandis, D, Chiarelli, F, Ferlini, A, Stuppia, L
Format:	Article
Language:	English
Subjects:	Abnormalities, Multiple - genetics Abnormalities, Multiple - pathology Esophageal Achalasia - genetics Esophageal Achalasia - pathology Female Humans Male Nerve Tissue Proteins - genetics Nuclear Pore Complex Proteins - genetics
Citations:	Items that this one cites Items that cite this one
Online Access:	Get full text
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