CC2D2A mutations in Meckel and Joubert syndromes indicate a...

Human Mutation 2009 Vol. 30; Iss. 11

CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype–phenotype correlation

Soumaya Mougou-Zerelli, Sophie Thomas, Emmanuelle Szenker, Sophie Audollent, Nadia Elkhartoufi, Candice Babarit, Stéphane Romano, Rémi Salomon, Jeanne Amiel, Chantal Esculpavit, Marie Gonzales, Estell
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Volume:
30
Year:
2009
Language:
english
Pages:
9
DOI:
10.1002/humu.21116
File:
PDF, 579 KB
english, 2009
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