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Continuous gene deletion syndrome in two families involving OTC, RPGR and TSPAN7 genes, presenting as ornithine transcarbamylase deficiency
✍ Scribed by Jain-Ghai, Shailly; Skinner, Stephanie; Hartley, Jessica; Greenberg, Cheryl; Chan, Alicia
- Book ID
- 126543170
- Publisher
- Elsevier Science
- Year
- 2014
- Tongue
- English
- Weight
- 58 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0009-9120
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