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A novel missense mutation in theEDAgene associated with X-linked recessive isolated hypodontia

✍ Scribed by Mahmood Rasool; Jens Schuster; Muhammad Aslam; Muhammad Tariq; Ilyas Ahmad; Amjad Ali; Miriam Entesarian; Niklas Dahl; Shahid Mahmood Baig


Publisher
Nature Publishing Group
Year
2008
Tongue
English
Weight
357 KB
Volume
53
Category
Article
ISSN
1435-232X

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## Abstract Most X‐linked diseases show a recessive pattern of inheritance in which female carriers are unaffected. In X‐linked retinitis pigmentosa (XLRP), however, both recessive and semi‐dominant inheritance patterns have been reported. We identified an Israeli family with semi‐dominant XLRP due