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Wiley, Human Mutation: Variation, Informatics and Disease, 5(42), p. 506-519, 2021

DOI: 10.1002/humu.24179

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Biallelic hypomorphic variants in ALDH1A2 cause a novel lethal human multiple congenital anomaly syndrome encompassing diaphragmatic, pulmonary, and cardiovascular defects

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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