Swallow, D M

Sialidosis type 1: cherry red spot-myoclonus syndrome with sialidase deficiency and altered electrophoretic mobility of some enzymes known to be glycoproteins. II. Enzymes studies. [electronic resource] - Annals of human genetics Jul 1979 - 27-35 p. digital

Publication Type: Journal Article

0003-4800


Adult
Ataxia--genetics
Electrophoresis
Glycoproteins--analysis
Humans
Hydrolases--analysis
Male
Myoclonus--enzymology
Neuraminidase--deficiency
Oligosaccharides--urine
Syndrome
Vision Disorders--genetics