Amylaceous (Polyglucosan) Bodies in Familial Cerebral Atrophy of Early Onset.
- Published in:
- Journal of Child Neurology, 1996, v. 11, n. 1, p. 58, doi. 10.1177/088307389601100115
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- Publication type:
- Article
Works matching AU Johnson, G. Stephan
Results: 2
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A novel and de novo spontaneous point mutation (Glu271STOP) of the antithrombin gene results in a type I deficiency and thrombophilia.
- Published in:
- American Journal of Hematology, 1999, v. 60, n. 2, p. 126, doi. 10.1002/(SICI)1096-8652(199902)60:2<126::AID-AJH7>3.0.CO;2-L
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- Publication type:
- Article