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Detection of a point mutation in sphingolipid activator protein-1 mRNA in patients with a variant form of metachromatic leukodystrophy

✍ Scribed by Mohammad A. Rafi; Xun-Ling Zhang; Gregory DeGala; David A. Wenger

Book ID: 115763067
Publisher: Elsevier Science
Year: 1990
Tongue: English
Weight: 645 KB
Volume: 166
Category: Article
ISSN: 0006-291X
DOI: 10.1016/0006-291x(90)90912-7

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