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Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain

Bibliographic reference Sen, Partha ; Yang, Yaping ; Navarro, Colby ; Silva, Iris ; Szafranski, Przemyslaw ; et. al. Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain. In: Human Mutation, Vol. 34, no. 6, p. 801-811 (2013)
Permanent URL http://hdl.handle.net/2078.1/151866
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