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Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3
✍ Scribed by Hu, Cougar Hao; Garshasbi, Masoud; Abedini, Seyedeh Sedigheh; Ghadami, Shirin; Kariminejad, Roxana; Ullmann, Reinhard; Chen, Wei; Ropers, H-Hilger; Kuss, Andreas W; Kahrizi, Kimia
- Book ID
- 109849233
- Publisher
- Nature Publishing Group
- Year
- 2010
- Tongue
- English
- Weight
- 230 KB
- Volume
- 19
- Category
- Article
- ISSN
- 1018-4813
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