Identification of SPOCK2 as a susceptibility gene for bronchopulmonary dysplasia.
Hadchouel A, Durrmeyer X, Bouzigon E et al.
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Abstract
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Rationale: Bronchopulmonary dysplasia is the most common chronic respiratory disease in premature infants. Genetic factors might contribute to bronchopulmonary dysplasia susceptibility.
22 European ancestry cases, 76 European ancestry controls, 21 African ancestry cases, 86 African ancestry controls
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