✦ LIBER ✦
P02-50 A new cause of GH deficiency: Mutation in the nuclear encoded mitochondrial isoleucyl tRNA-synthetase (IARS2) in 3 patients with severe short stature, cataracts and peripheral neuropathy
✍ Scribed by Deal, C.; Desilets, V.; Patry, L.; Cavanagh-Papillon, S.; Majewski, J.; Michaud, J.; Shoubridge, E.; Samuels, M.E.
- Book ID
- 122642131
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 67 KB
- Volume
- 22
- Category
- Article
- ISSN
- 1096-6374
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