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APA Citation
Ullah, A., Raza, S. I., Ali, R. H., Naveed, A. K., Jan, A., Rizvi, S. D. A., Satti, R., & Ahmad, W. (2015). a novel deletion mutation in the DSG4 gene underlies autosomal recessive hypotrichosis with variable phenotype in two unrelated consanguineous families. Clinical and experimental dermatology, 40, 78–84. http://access.bl.uk/ark:/81055/vdc_100172213061.0x00000b