Identification of CC2D2A as a Meckel Syndrome Gene Adds an Important Piece to the Ciliopathy Puzzle
Open Access
- 6 June 2008
- journal article
- case report
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 82 (6), 1361-1367
- https://doi.org/10.1016/j.ajhg.2008.05.004
Abstract
No abstract availableThis publication has 89 references indexed in Scilit:
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