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Deletion of the last two exons of FGF10 in a family with LADD syndrome and pulmonary acinar hypoplasia
Pulmonary acinar hypoplasia (PAH) and lacrimo-auriculo-dento-digital (LADD) syndrome have both been associated with loss-of-function variants in, or deletions of FGF10. Here we report a multi-generational family with seven members manifesting varying features of LADD syndrome, with one individual dy...
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| Pubblicato in: | Eur J Hum Genet |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Springer International Publishing
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8106901/ https://ncbi.nlm.nih.gov/pubmed/33967277 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-021-00902-0 |
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