๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

The C282Y haemochromatosis mutation is associated with osteoporosis in heterozygous and homozygous subjects

โœ Scribed by Jenny Gunton; Fran Gates; Greg Fulcher; Phillip Clifton-Bligh


Book ID
117807187
Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
103 KB
Volume
27
Category
Article
ISSN
8756-3282

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


A novel splice site mutation in the SPG7
โœ Tobias Warnecke; Thomas Duning; Anja Schirmacher; Siawoosh Mohammadi; Wolfram Sc ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 285 KB

## Abstract Hereditary spastic paraplegias (HSP) are genetically and clinically heterogeneous neurodegenerative disorders. The purpose of this study was to assess the genotype and phenotype in a family with a complicated form of autosomal recessive hereditary spastic paraplegia (ARHSP). Neurologica