CRS4

Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene.

Teresa Esposito, RA Lea, BH Maher, D Moses, HC Cox, S Magliocca, Andrea Angius, DR Nyholt, T Titus, T Kay, NA Gray, NP Rastaldi, A Pamham, Fernando Gianfrancesco, LR Griffiths
Human Molecular Genetics, Volume 22 (18), page 3654-66 - may 2013

Références BibTex

@Article{ELMMCMANTKGRPGG13,
  author       = {Esposito, T. and Lea, R. and Maher, B. and Moses, D. and Cox, H. and Magliocca, S. and Angius, A. and Nyholt, D. and Titus, T. and Kay, T. and Gray, N. and Rastaldi, N. and Pamham, A. and Gianfrancesco, F. and Griffiths , L.},
  title        = {Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene.},
  journal      = {Human Molecular Genetics},
  volume       = {22 (18)},
  pages        = {3654-66},
  month        = {may},
  year         = {2013},
  publisher    = {springer},
  keywords     = {X-linked familial FSGS,Heart block disorder, XF5 gene},
  doi          = {10.1093/hmg/ddt215},
  url          = {http://publications.crs4.it/pubdocs/2013/ELMMCMANTKGRPGG13},
}

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