Novel point mutation in the NKX2-5 gene in a Moroccan family with atrioventricular conduction disturbance and an atrial septal defect in the oval fossa (Q39398648)
Jump to navigation
Jump to search
scientific article published on 22 December 2006
Language | Label | Description | Also known as |
---|---|---|---|
English | Novel point mutation in the NKX2-5 gene in a Moroccan family with atrioventricular conduction disturbance and an atrial septal defect in the oval fossa |
scientific article published on 22 December 2006 |
Statements
1 reference
Novel point mutation in the NKX2-5 gene in a Moroccan family with atrioventricular conduction disturbance and an atrial septal defect in the oval fossa (English)
1 reference
Laïla Rifai
1 reference
Wajih Maazouzi
1 reference
Abdelaziz Sefiani
1 reference
22 December 2006
1 reference
1 reference
17
1 reference
1
1 reference
107-109
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference