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| Number | Title | Issue Date |
| 8119351 | CC2D2A gene mutations associated with Joubert syndrome and diagnostic methods for identifying the same The present invention provides a method of screening a subject for mutations in the CC2D2A gene that are associated with Joubert syndrome, an autosomal recessive form of mental retardation. The present invention also provides proteins that are associated with Jouber... | 02/21/2012 |
| 7670773 | MECP2E1 gene The invention is a novel MECP2E1 splice variant and its corresponding polypeptide. The invention also includes methods of using these nucleic acid sequences and proteins in medical diagnosis and treatment of neuropsychiatric disorders or development disorders. ... | 03/02/2010 |
