๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

The reliability of death certification in patients dying with mucopolysaccharidosis type II (Hunter syndrome)

โœ Scribed by D Seshadri; S Jones; K Burt; L Lavery; JE Wraith


Book ID
110889199
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
472 KB
Volume
79
Category
Article
ISSN
0009-9163

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Mutations of the iduronate-2-sulfatase g
โœ Ewa Popowska; Michaela Rathmann; Anna Tylki-Szymanska; Susanna Bunge; Cordula St ๐Ÿ“‚ Article ๐Ÿ“… 1995 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 478 KB ๐Ÿ‘ 1 views

## Communicated by Francesco Giannelli Mucopolysaccharidosis type I1 (MI'S 11) is an X-chromosomal storage disorder due to deficiency of the lysosomal enzyme iduronate-2-sulfatase

Two New Nonsense mutations (Q80X; Q389X)
โœ Romeo Carrozzo; Rossana Tonlorenzi; Fabio Corsolini; Rosanna Gatti ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 192 KB ๐Ÿ‘ 1 views

More than 100 mutations of the HPRT gene have been described related to Lesch-Nyhan syndrome in complete lack of enzyme activity, or KelleySeegmiller syndrome in partial enzyme deficiency. We examined (modified according to genomic DNA from an 11-year-old boy, S.Z., with -1% HPRT activity, who had