CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation
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author: Tania Attié-Bitach, Michel Vekemans, Jeanne Amiel, Sophie Saunier, Enza Maria Valente, Nathalie Boddaert, Arnold Munnich, Anne-Lise Delezoide, Sylvie Odent, Marie-Pierre Cordier, Férechté Encha-Razavi, Soumaya Mougou-Zerelli, Marie-Claire Gubler, Sophie Thomas, Meriam Hadj Amor, Sophie Patrier, Nadia Elkhartoufi, Sophie Audollent, Candice Babarit, Philippe Loget, Joelle Roume
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