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...
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| Main Authors: | , , |
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| Format: | Book |
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The Company of Biologists,
2015-09-01T00:00:00Z.
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