A first case report of hypohidrotic ectodermal dysplasia from Oman
Abstract This is a first case report of a patient with hypohidrotic ectodermal dysplasia from Oman, who was found to carry a mutation in the EDAR gene after candidate gene selection based on regions of homozygosity in his genome.
| Päätekijät: | , , , |
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| Aineistotyyppi: | Artikkeli |
| Kieli: | English |
| Julkaistu: |
Wiley
2020-04-01
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| Sarja: | Clinical Case Reports |
| Aiheet: | |
| Linkit: | https://doi.org/10.1002/ccr3.2723 |