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De Novo ACTG1 Variant Expands the Phenotype and Genotype of Partial Deafness and Baraitser-Winter Syndrome
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Published in: | International journal of molecular sciences 2022, Vol.23 (2) |
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Main Authors: | , , , , , , , , , |
Format: | Report |
Language: | English |
Online Access: | Get full text |
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ISSN: | 1422-0067 |
DOI: | 10.3390/ijms23020692 |