Caricamento...

Variable expression of osteogenesis imperfecta in a nuclear family is explained by somatic mosaicism for a lethal point mutation in the alpha 1(I) gene (COL1A1) of type I collagen in a parent.

Fibroblasts from a man with a mild form of osteogenesis imperfecta (OI) and from his son with perinatal lethal OI (OI type II) produced normal and abnormal type I procollagen molecules. The abnormal molecules synthesized by both cell strains contained one or two pro alpha 1(I) chains in which the gl...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Autori principali: Wallis, G A, Starman, B J, Zinn, A B, Byers, P H
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1990
Soggetti:
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683813/
https://ncbi.nlm.nih.gov/pubmed/2339700
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !