Ophthalmic Manifestations of Danon Disease
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference11 articles.
1. Lysosomal glycogen storage disease with normal acid maltase;Danon;Neurology,1981
2. Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease);Nishino;Nature,2000
3. Two human lysosomal membrane glycoproteins, h-lamp-1 and h-lamp-2, are encodes by genes localized to chromosome13q34 and chromosome Xq24-25, respectively;Mattei;J Biol Chem,1990
4. Accumulation of autophagic vacuoles and cadiomyopathy in LAMP-2–deficient mice;Tanaka;Nature,2000
5. Clinicopathological features of genetically confirmed Danon disease;Sugie;Neurology,2002
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2. Multisystem involvement and early onset of Danon’s disease in female children. Clinical cases;Translational Medicine;2024-06-20
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