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Autor:
Tuğçe N. Pekdemir, Duygu Öztürk, Merve T. Çetindağ, Ebru Akleyn, Cansu O. Sarıyıldız, Michele Callea, İzzet Yavuz
Publikováno v:
Makara Journal of Health Research, Vol 22, Iss 2, Pp 63-68 (2018)
Hutchinson-Gilford progeria syndrome (HGPS) is a rare autosomal recessive genetic disorder that occurs as a point mutation in the LMNA gene. It is a rare hereditary disorder, with approximately 100 cases reported in the medical literature. These pati
Externí odkaz:
https://doaj.org/article/0c5d039cef514f198c47e20223588647
