Eighteen novel mutations in patients with Lesch–Nyhan syndrome or partial hypoxanthine phosphoribosy...
Eighteen novel mutations in patients with Lesch–Nyhan syndrome or partial hypoxanthine phosphoribosyltransferase deficiency
About this item
Full title
Eighteen novel mutations in patients with Lesch–Nyhan syndrome or partial hypoxanthine phosphoribosyltransferase deficiency
Author / Creator
Willers, I. , Bolz, H. , Wehnert, M. and Gal, A.
Publisher
Dordrecht: Kluwer Academic Publishers
Journal title
Journal of inherited metabolic disease, 1999-10, Vol.22 (7), p.845-846
Language
English
Formats
Publication information
Publisher
Dordrecht: Kluwer Academic Publishers
Subjects
More information
Alternative Titles
Full title
Eighteen novel mutations in patients with Lesch–Nyhan syndrome or partial hypoxanthine phosphoribosyltransferase deficiency
Authors, Artists and Contributors
Author / Creator
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_70829180
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_70829180
Other Identifiers
ISSN
0141-8955
E-ISSN
1573-2665
DOI
10.1023/A:1005522527689
