DOI:
10.1055/s-00000034
Klinische Pädiatrie
LinksClose Window
References
Ullah A, Raza SI, Ali RH. et al.
A novel deletion mutation in the DSG4 gene underlies autosomal recessive
hypotrichosis with variable phenotype in two unrelated consanguineous
families.
Clin Exp Dermatol 2015;
40: 78-84
We do not assume any responsibility for the contents of the web pages of other providers.