A novel deletion mutation in theDSG4gene underlies autosomal recessive hypotrichosis with variable phenotype in two unrelated consanguineous families
Clinical and Experimental Dermatology2014Vol. 40(1), pp. 78–84
Citations Over TimeTop 14% of 2014 papers
Asmat Ullah, Syed Irfan Raza, Raja Hussain Ali, A. Naveed, Abid Jan, S. D. A. Rizvi, R. Satti, Wasim Ahmad
Abstract
This study further extends the body of evidence that mutations in the DSG4 gene result in both hypotrichosis and monilethrix-like scalp hair.
Related Papers
- → Consanguinity and reproductive health among Arabs(2009)622 cited
- → Consanguinity among the Saudi Arabian population.(1995)464 cited
- → The Bazex-Dupré-Christol Syndrome(1994)74 cited
- → Consanguinity associated with increased risk for bipolar I disorder in Egypt(2009)31 cited
- Further delineation of the hypotrichosis-deafness syndrome.(2006)