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Conference Paper: Role of epigenetic dysregulation in neurodevelopmental syndromes: lessons from KDM5C mutations
| Title | Role of epigenetic dysregulation in neurodevelopmental syndromes: lessons from KDM5C mutations |
|---|---|
| Authors | |
| Keywords | Epigenetics KW109 - Methylation KW123 - Neurogenetics KW181 - X-Linked Disease KW106 - Mental Retardation |
| Issue Date | 2011 |
| Publisher | ICHG/ASHG 2011. |
| Citation | The 2011 Joint Meeting of the International Congress of Human Genetics (ICHG) and American Society of Human Genetics (ASHG), Montreal, QC., Canada, 11-15 October 2011. How to Cite? |
| Abstract | Genes encoding proteins that function in epigenetic modification play an important role in normal neurodevelopment. However, the molecular mechanisms that underpin hierarchical epigenetic marks and drive normal development are not well understood. Human diseases caused by mutations in genes that modify epigenetic marks provide a uni... |
| Description | Poster Session - Epigenetics: program no. 762T: abstract no. 10741 |
| Persistent Identifier | http://hdl.handle.net/10722/143411 |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Grafodatskaya, D | en_US |
| dc.contributor.author | Chung, BHY | en_US |
| dc.contributor.author | Butcher, DT | en_US |
| dc.contributor.author | Goodman, S | en_US |
| dc.contributor.author | Choufan, S | en_US |
| dc.contributor.author | Lou, Y | en_US |
| dc.contributor.author | Zhao, C | en_US |
| dc.contributor.author | Rajendram, R | en_US |
| dc.contributor.author | Abidi, FE | en_US |
| dc.contributor.author | Skinner, C | en_US |
| dc.contributor.author | Hamilton, J | en_US |
| dc.contributor.author | Scherer, SW | en_US |
| dc.contributor.author | Schwartz, CE | en_US |
| dc.contributor.author | Weksberg, R | en_US |
| dc.date.accessioned | 2011-11-24T10:06:40Z | - |
| dc.date.available | 2011-11-24T10:06:40Z | - |
| dc.date.issued | 2011 | en_US |
| dc.identifier.citation | The 2011 Joint Meeting of the International Congress of Human Genetics (ICHG) and American Society of Human Genetics (ASHG), Montreal, QC., Canada, 11-15 October 2011. | en_US |
| dc.identifier.uri | http://hdl.handle.net/10722/143411 | - |
| dc.description | Poster Session - Epigenetics: program no. 762T: abstract no. 10741 | - |
| dc.description.abstract | Genes encoding proteins that function in epigenetic modification play an important role in normal neurodevelopment. However, the molecular mechanisms that underpin hierarchical epigenetic marks and drive normal development are not well understood. Human diseases caused by mutations in genes that modify epigenetic marks provide a uni... | - |
| dc.language | eng | en_US |
| dc.publisher | ICHG/ASHG 2011. | - |
| dc.relation.ispartof | ICHG-ASHG 2011 Joint Meeting | en_US |
| dc.subject | Epigenetics | - |
| dc.subject | KW109 - Methylation | - |
| dc.subject | KW123 - Neurogenetics | - |
| dc.subject | KW181 - X-Linked Disease | - |
| dc.subject | KW106 - Mental Retardation | - |
| dc.title | Role of epigenetic dysregulation in neurodevelopmental syndromes: lessons from KDM5C mutations | en_US |
| dc.type | Conference_Paper | en_US |
| dc.identifier.email | Chung, BHY: bhychung@hku.hk | en_US |
| dc.identifier.authority | Chung, BHY=rp00473 | en_US |
| dc.description.nature | link_to_OA_fulltext | - |
| dc.identifier.hkuros | 197765 | en_US |
| dc.publisher.place | United States | - |