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Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome
Authors
Bertini E, Dallapiccola B, Gleeson JG International Joubert Syndrome Related Disorders Study Group
Silhavy JL, Brancati F, Barrano G, Krishnaswami SR, Castori M, Lancaster MA, Boltshauser E, Boccone L, Al-Gazali L, Fazzi E, Signorini S, Louie CM, Bellacchio E Valente EM
Publication date
Publisher
Nature America Incorporated:345 Park Avenue South, 6th Floor:New York, NY 10010:(888)331-6288, EMAIL:
[email protected]
, INTERNET: http://www.nature.com, Fax: (212)689-9108
Abstract
Abstract is not available.
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Archivio Istituzionale della Ricerca - Università degli Studi di Pavia
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oai:iris.unipv.it:11571/106544
Last time updated on 03/09/2019
