Loading...

Introduction of a Phe377del Mutation in ANK Creates a Mouse Model for Craniometaphyseal Dysplasia

Craniometaphyseal dysplasia (CMD) is a monogenic human disorder characterized by thickening of craniofacial bones and flaring metaphyses of long bones. Mutations for autosomal dominant CMD have been identified in the progressive ankylosis gene ANKH. Previous studies of Ank loss-of-function models, A...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Chen, I-Ping, Wang, Chiachien J., Strecker, Sara, Koczon-Jaremko, Boguslawa, Boskey, Adele, Reichenberger, Ernst J.
Format: Artigo
Sprog:Inglês
Udgivet: Amer Soc Bone & Mineral Res. 2009
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2697624/
https://ncbi.nlm.nih.gov/pubmed/19257826
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1359/JBMR.090218
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!