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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...

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Sonraí Bibleagrafaíochta
Main Authors: Collod, G, Béroud, C, Soussi, T, Junien, C, Boileau, C
Formáid: Artigo
Teanga:Inglês
Foilsithe: 1996
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC145600/
https://ncbi.nlm.nih.gov/pubmed/8594563
Clibeanna: Cuir Clib Leis
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