𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Germline mutations in the thyrotropin receptor gene cause non–autoimmune autosomal dominant hyperthyroidism

✍ Scribed by Duprez, Laurence; Parma, Jasmine; Van Sande, Jacqueline; Allgeier, Anouk; Leclère, Jacques; Schvartz, Claire; Delisle, Marie-Joëlle; Decoulx, Marc; Orgiazzi, Jacques; Dumont, Jacques


Book ID
109916454
Publisher
Nature Publishing Group
Year
1994
Tongue
English
Weight
746 KB
Volume
7
Category
Article
ISSN
1061-4036

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Mutations of the EPHA2 receptor tyrosine
✍ Tianxiao Zhang; Rui Hua; Wei Xiao; Kathryn P. Burdon; Shomi S. Bhattacharya; Jam 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 520 KB

Congenital cataracts (CCs) are clinically and genetically heterogeneous. Mutations in the same gene may lead to CCs differing in inheritance, morphology and severity. Loci for autosomal dominant posterior polar CC and total CC have both been mapped to the chromosomal 1p36 region harboring the EPHA2