Αρχειοθήκη ιστολογίου

Τετάρτη 29 Αυγούστου 2018

DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development

Bouilly, J; Messina, A; Papadakis, G; Cassatella, D; Xu, C; Acierno, JS; Tata, B; ... Pitteloud, N; + view all Bouilly, J; Messina, A; Papadakis, G; Cassatella, D; Xu, C; Acierno, JS; Tata, B; Sykiotis, G; Santini, S; Sidis, Y; Elowe-Gruau, E; Phan-Hug, F; Hauschild, M; Bouloux, P-M; Quinton, R; Lang-Muritano, M; Favre, L; Marino, L; Giacobini, P; Dwyer, AA; Niederlander, NJ; Pitteloud, N; - view fewer (2018) DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development. Human Molecular Genetics , 27 (2) pp. 359-372. 10.1093/hmg/ddx408 .

https://ift.tt/2PdvNM4

Δεν υπάρχουν σχόλια:

Δημοσίευση σχολίου