✦ LIBER ✦
Lipoprotein lipase (LPL) deficiency: a new patient homozygote for the preponderant mutation Gly188Glu in the human LPL gene and review of reported mutations: 75 % are clustered in exons 5 and 6
✍ Scribed by Brigitte Gilbert; Mustapha Rouis; Sabine Griglio; Lionel de Lumley; Paul-Michel Laplaud
- Book ID
- 113987229
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 105 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0003-3995
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