✦ LIBER ✦

P.3.009 Exploration of biological circadian rhythms in a patient with autism and a loss-of-function mutation of melatonin receptor type I

✍ Scribed by C. Pagan; P. Chaste; R. Delorme; X. Drouot; D. Chevenne; J.M. Launay; T. Bourgeron

Book ID: 118598861
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 66 KB
Volume: 22
Category: Article
ISSN: 0924-977X
DOI: 10.1016/s0924-977x(12)70062-7

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Immortalization and Characterization of

Immortalization and Characterization of Bone Marrow Stromal Fibroblasts from a Patient with a Loss of Function Mutation in the Estrogen Receptor-α Gene

✍ S. C. Dieudonné; T. Xu; J. Y. Chou; S. A. Kuznetsov; K. Satomura; M. Mankani; N. 📂 Article 📅 1998 🏛 American Society for Bone and Mineral Research 🌐 English ⚖ 373 KB

A(870)E mutation of the androgen recepto

A(870)E mutation of the androgen receptor gene in a patient with complete androgen insensitivity syndrome and sertoli cell tumor

✍ I Knoke; S Jakubiczka; T Ottersen; A Göppinger; P Wieacker 📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 919 KB

Sequence of exons and the flanking regio

Sequence of exons and the flanking regions of human bilirubin-UDP-glucuronosyltransferase gene complex and identification of a genetic mutation in a patient with Crigler-Najjar syndrome, type I

✍ Piter J. Bosma; Namita Roy Chowdhury; Bart G. Goldhoorn; Martin H. Hofker; Ronal 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 814 KB

Crigler-Najjar syndrome, type I is a heterogeneous