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Auditory hair cell defects as potential cause for sensorineural deafness in Wolf-Hirschhorn syndrome
WHSC1 is a histone methyltransferase (HMT) that catalyses the addition of methyl groups to lysine 36 on histone 3. In humans, WHSC1 haploinsufficiency is associated with all known cases of Wolf-Hirschhorn syndrome (WHS). The cardinal feature of WHS is a craniofacial dysmorphism, which is accompanied...
Kaydedildi:
| Yayımlandı: | Dis Model Mech |
|---|---|
| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
The Company of Biologists
2015
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4582100/ https://ncbi.nlm.nih.gov/pubmed/26092122 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.019547 |
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