Coinheritance of two rare genodermatoses (Papillon-Lefevre syndrome and oculocutaneous albinism type 1) in two families: a genetic study
Chelsee Hewitt(St. Mary's Hospital), Nalin Thakker(University Dental Hospital of Manchester), Philip Sloan(Newcastle University), Khaled Abdel Ghaffar(Ain Shams University), Jacqueline A. James(Queen's University Belfast), C-L. Wu(University of Manchester), Faiez N. Hattab, Wala M. Amin(University of Jordan), Andrew Read(University of Manchester), Carmel Toomes(University of Leeds)
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