Yazar "Karapapak, Murat" için listeleme
-
Hypotrichosis and Juvenile Macular Dystrophy-First Homozygous Family Case from Turkiye
Caf, Nazlı; Gezdirici, Alper; Karapapak, Murat; Kırsoy, Erişcan Melih; Çetinkaya, Elif; Yılmaz, Halil İbrahim; Türkoğlu, Zafer (GALENOS PUBL HOUSE, 2025)Hypotrichosis with juvenile macular dystrophy (HMJD) is a rare autosomal recessive disease that leads to blindness in the first thirty years of life. It is characterized by hypotrichosis and progressive macular degeneration. ...