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A novel stop mutation truncating critical regions of the cardiac transcription factor NKX2-5 in a large family with autosomaldominant inherited congenital heart disease

✍ Scribed by S. Pabst; B. Wollnik; E. Rohmann; Y. Hintz; K. Glänzer; H. Vetter; G. Nickenig; Christian Grohé


Publisher
Springer
Year
2007
Tongue
English
Weight
181 KB
Volume
97
Category
Article
ISSN
1861-0684

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