Small partial deletion of a highly GC-rich FOXF1 exon 1 in two deceased siblings with alveolar capillary dysplasia

SSRN Electronic Journal 2026 Preprint Open access

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Authors: Pawel Stankiewicz, Hiuling Chan Joiner, Ms. Shruti Pande, Przemyslaw Szafranski, Partha Sen, G Deutsch

DOI: 10.2139/ssrn.6018307

Cited by: 0

Fields of Study & Subjects

Tuberous Sclerosis Complex Research Genomics and Rare Diseases Neonatal Respiratory Health Research