Two clinical forms of glycogen-storage disease type II in two generations of the same family
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2005.00557.x/fullpdf
Reference15 articles.
1. Adult acid maltase deficiency;Barohn;Muscle Nerve,1993
2. Phenotypic expression of late-onset glycogen storage disease type II: identification of asymptomatic adults through family studies and review of reported families;Ausems;Neuromuscul Disord,2000
3. Glycogenosis type II. The infantile and late-onset acid maltase deficiency observed in one family;Koster;Clin Chim Acta,1978
4. A family with different clinical forms of acid maltase deficiency (glycogenosis type II): biochemical and genetic studies;Loonen;Neurology,1981
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