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Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants
Contributors
- Griffin, Helen R.
- Töpf, Ana
- Glen, Elise
- Zweier, Christiane
- Stuart, A. Graham
- Parsons, Jonathan
- Peart, Ian
- Deanfield, John
- O'Sullivan, John
- Rauch, Anita
- …
Subject
- Medizin, Gesundheit
- -
- -
Contributors
- Griffin, Helen R.
- Töpf, Ana
- Glen, Elise
- Zweier, Christiane
- Stuart, A. Graham
- Parsons, Jonathan
- Peart, Ian
- Deanfield, John
- O'Sullivan, John
- Rauch, Anita
- …
Subject
- Medizin, Gesundheit
- -
- -
Providing institution
Aggregator
Rights statement for the media in this item (unless otherwise specified)
- http://rightsstatements.org/vocab/InC/1.0/
Identifier
- http://nbn-resolving.de/urn:nbn:de:bvb:29-opus4-63962
Language
- eng
Providing country
- Germany
Collection name
First time published on Europeana
- 2017-04-05T13:05:32.108Z
Last time updated from providing institution
- 2017-11-13T10:24:09.322Z