AHMAD, F., AHMED, I., NASIR, A., UMAIR, M., SHAHZAD, S., MUHAMMAD, D., . . . AHMAD, W. (2018). A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family. Eur J Dermatol.
Chicago Stili AlıntıAHMAD, Farooq, Ishtaiq AHMED, Abdul NASIR, Muhammad UMAIR, Shaheen SHAHZAD, Dost MUHAMMAD, Regie Lyn P. SANTOS-CORTEZ, Suzanne M. LEAL, ve Wasim AHMAD. "A Disease-causing Novel Missense Mutation in the ST14 Gene Underlies Autosomal Recessive Ichthyosis With Hypotrichosis Syndrome in a Consanguineous Family." Eur J Dermatol 2018.
MLA AlıntıAHMAD, Farooq, et al. "A Disease-causing Novel Missense Mutation in the ST14 Gene Underlies Autosomal Recessive Ichthyosis With Hypotrichosis Syndrome in a Consanguineous Family." Eur J Dermatol 2018.