Biochemical investigations of cultured amniotic fluid cells in mucolipidosis type IV
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference19 articles.
1. Congenital corneal clouding with abnormal systemic storage bodies: A new variant of mucolipidosis
2. A New Mucolipidosis with Psychomotor Retardation, Corneal Clouding, and Retinal Degeneration
3. Mucolipidosis IV
4. Abnormal ganglioside accumulation in cultured fibroblasts from patients with mucolipidosis IV
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1. The role of TRPMLs in endolysosomal trafficking and function;Cell Calcium;2015-07
2. Lysosomal Ca2+ homeostasis: Role in pathogenesis of lysosomal storage diseases;Cell Calcium;2011-08
3. Mucolipidosis Type IV;Molecular Genetics and Metabolism;2001-07
4. Mucolipidosis type IV: A mild form with late onset;American Journal of Medical Genetics;1993-09-01
5. Detection of complex gangliosides in human amniotic fluid;FEBS Letters;1993-08-09
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