WOLMAN-DISEASE DUE TO HOMOZYGOSITY FOR A NOVEL TRUNCATED VARIANT OF LYSOSOMAL ACID LIPASE (351INSA) ASSOCIATED WITH COMPLETE IN-SITU ACID LIPASE DEFICIENCY

Authors
SEEDORF U HEIKO W SANDRO M ERTAN M HARALD F GERD A
Citation
U. Seedorf et al., WOLMAN-DISEASE DUE TO HOMOZYGOSITY FOR A NOVEL TRUNCATED VARIANT OF LYSOSOMAL ACID LIPASE (351INSA) ASSOCIATED WITH COMPLETE IN-SITU ACID LIPASE DEFICIENCY, Circulation, 94(8), 1996, pp. 196-196
Citations number
NO
Categorie Soggetti
Cardiac & Cardiovascular System",Hematology
Journal title
Circulation → ACNP
ISSN journal
00097322
Volume
94
Issue
8
Year of publication
1996
Supplement
S
Pages
196 - 196
Database
ISI
SICI code
0009-7322(1996)94:8<196:WDTHFA>2.0.ZU;2-F