The Opitz syndrome gene product, MID1, associates with microtubules

Opitz syndrome (OS) is a genetically heterogeneous disorder characterized by defects of the ventral midline, including hypertelorism, cleft lip and palate, heart defects, and mental retardation. We recently identified the gene responsible for X-linked OS. The ubiquitously expressed gene product, MID...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Schweiger, Susann, Foerster, John, Lehmann, Tanja, Suckow, Vanessa, Muller, Yves A., Walter, Gerald, Davies, Theresa, Porter, Helen, van Bokhoven, Hans, Lunt, Peter W., Traub, Peter, Ropers, Hans-Hilger
Format: Artigo
Sprog:Inglês
Udgivet: The National Academy of Sciences 1999
Fag:
Biological Sciences
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC15848/
https://ncbi.nlm.nih.gov/pubmed/10077590
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker