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CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders.

Academic Article
Publication Date:
2007
Iris type:
1.1 Articolo in rivista
Keywords:
Joubert syndrome-related disorders; CEP290 mutations
List of contributors:
Brancati, F; Barrano, G; Silhavy, Jl; Marsh, Se; Travaglini, L; Bielas, Sl; Amorini, M; Zablocka, D; Kayserili, H; AL GAZALI, L; Bertini, E; Boltshauser, E; D'Hooghe, M; Fazzi, ELISA MARIA; Fenerci, Ey; Hennekam, Rc; Kiss, A; Lees, Mm; Marco, E; Phadke, Sr; Rigoli, L; Romano, S; Salpietro, Cd; Sherr, Eh; Signorini, S; Stromme, P; Stuart, B; Sztriha, L; Viskochil, Dh; Yuksel, A; Dallapiccola, B; INTERNATIONAL JSRD STUDY, Group; Valente, ENZA MARIA; Gleeson, Jg
Authors of the University:
VALENTE ENZA MARIA
Handle:
https://iris.unipv.it/handle/11571/106547
Published in:
AMERICAN JOURNAL OF HUMAN GENETICS
Journal
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