Recurrent mutations in functionally-relatedEDAandEDARgenes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasia

✍ Scribed by Zahid Azeem; Syed Kamran-Ul-Hassan Naqvi; Muhammad Ansar; Abdul Wali; Abdul Khaliq Naveed; Ghazanfar Ali; Muhammad Jawad Hassan; Muhammad Tariq; Sulman Basit; Wasim Ahmad

• Publisher: Springer-Verlag
• Year: 2009
• Tongue: English
• Weight: 350 KB
• Volume: 301
• Category: Article
• ISSN: 0340-3696
• DOI: 10.1007/s00403-009-0975-1