APA

Swallow D. M., Evans L., Stewart G., Thomas P. K. & Abrams J. D. (19791227). 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. : Annals of human genetics.

Chicago

Swallow D M, Evans L, Stewart G, Thomas P K and Abrams J D. 19791227. 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. : Annals of human genetics.

Harvard

Swallow D. M., Evans L., Stewart G., Thomas P. K. and Abrams J. D. (19791227). 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. : Annals of human genetics.

MLA

Swallow D M, Evans L, Stewart G, Thomas P K and Abrams J D. 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. : Annals of human genetics. 19791227.