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Vanier M.T., Ferlinz K., Rousson R., Duthel S., Louisot P., Sandhoff K., Suzuki K. Deletion of arginine (608) in acid sphingomyelinase is the prevalent mutation among Niemann-Pick disease type B patients from northern Africa. - Hum.Genet., 1993, v. 92, p. 325-330.
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