FBN1 c.1416C>A ;(p.C472*)

Variant ID: 15-48807636-G-T

NM_000138.4(FBN1):c.1416C>A;(p.C472*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 gene.

European Journal Of Human Genetics : Ejhg
Stheneur, Chantal C; Collod-Béroud, Gwenaëlle G; Faivre, Laurence L; Buyck, Jean François JF; Gouya, Laurent L; Le Parc, Jean-Marie JM; Moura, Bertrand B; Muti, Christine C; Grandchamp, Bernard B; Sultan, Gilles G; Claustres, Mireille M; Aegerter, Philippe P; Chevallier, Bertrand B; Jondeau, Guillaume G; Boileau, Catherine C
Publication Date: 2009-09

Variant appearance in text: FBN1: 1416C>A
PubMed Link: 19293843
Variant Present in the following documents:
  • Main text
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