Clinical, pathological, and biochemical studies on an infantile case of sulfatide/GM1 activator protein deficiency
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference30 articles.
1. Intraneuronal lipid deposits in metachromatic leukodystrophy: Histochemical and topographic observations
2. Four cases of late onset metachromatic leucodystrophy in a family: clinical, biochemical and neuropathological studies.
3. Studies in Metachromatic Leukodystrophy
4. Biosynthesis and molecular cloning of sulfated glycoprotein 1 secreted by rat Sertoli cells: sequence similarity with the 70-kilodalton precursor to sulfatide/GM1 activator
5. CHEMICAL COMPOSITIONS OF BRAIN AND MYELIN IN TWO PATIENTS WITH MULTIPLE SULPHATASE DEFICIENCY (A VARIANT FORM OF METACHROMATIC LEUKODYSTROPHY)
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