Identification of rare causal variants in sequence-based studies: Methods and applications to gene VPS13B, involved in Cohen syndrome and autism Meeting Abstract
| Authors: | Ionita-Laza, I.; Capanu, M.; De Rubeis, S.; McCallum, K.; Buxbaum, J. |
| Abstract Title: | Identification of rare causal variants in sequence-based studies: Methods and applications to gene VPS13B, involved in Cohen syndrome and autism |
| Meeting Title: | 42nd European Mathematical Genetics Meeting (EMGM) |
| Journal Title: | Human Heredity |
| Volume: | 76 |
| Issue: | 2 |
| Meeting Dates: | 2014 Apr 1-2 |
| Meeting Location: | Cologne, Germany |
| ISSN: | 0001-5652 |
| Publisher: | S. Karger AG |
| Date Published: | 2013-01-01 |
| Start Page: | 93 |
| Language: | English |
| ACCESSION: | WOS:000333337100023 |
| PROVIDER: | wos |
| Notes: | Meeting Abstract: O-15 -- 42nd European Mathematical Genetics Meeting (EMGM) -- APR 01-02, 2014 -- Cologne, GERMANY -- Source: Wos |
MSK Authors
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388Capanu