Novel missense mutation in the RSPO4 gene in congenital hyponychia and evidence for a polymorphic initiation codon (p.M1I).
| Autor: | Khan, Tahir Naeem1, Klar, Joakim2, Nawaz, Sadia1, Jameel, Muhammad1, Tariq, Muhammad1, Malik, Naveed Altaf1, Baig, Shahid M1, Dahl, Niklas2 niklas.dahl@igp.uu.se |
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| Zdroj: | BMC Medical Genetics. 2012, Vol. 13 Issue 1, p120-124. 5p. 1 Color Photograph, 1 Diagram. |
| Databáze: | Academic Search Ultimate |
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