Juvenile spinal muscular atrophy: A new hexosaminidase deficiency phenotype.

Autor: Johnson, William G., Wigger, H. Joachim, Karp, Herbert R., Glaubiger, Lawrence M., Rowland, Lewis P.
Zdroj: Annals of Neurology; 1982, Vol. 11 Issue 1, p11-16, 6p
Databáze: Complementary Index
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