Učitavanje...

Software and database for the analysis of mutations in the human FBN1 gene.

Fibrillin is the major component of extracellular microfibrils. Mutations in the fibrillin gene on chromosome 15 (FBN1) were described at first in the heritable connective tissue disorder, Marfan syndrome (MFS). More recently, FBN1 has also been shown to harbor mutations related to a spectrum of con...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Glavni autori: Collod, G, Béroud, C, Soussi, T, Junien, C, Boileau, C
Format: Artigo
Jezik:Inglês
Izdano: 1996
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC145600/
https://ncbi.nlm.nih.gov/pubmed/8594563
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!