An unusual mutation in the XPG gene leads to an internal in-frame deletion and a XP/CS complex phenotype

✍ Scribed by Lehmann, J.; Schubert, S.; Schäfer, A.; Apel, A.; Laspe, P.; Schiller, S.; Ohlenbusch, A.; Gratchev, A.; Emmert, S.

• Book ID: 121798427
• Publisher: John Wiley and Sons
• Year: 2014
• Tongue: English
• Weight: 208 KB
• Volume: 171
• Category: Article
• ISSN: 0007-0963
• DOI: 10.1111/bjd.13035