Elaborating the phenotypic spectrum associated with mutations in ARFGEF2: Case study and literature review - Archive ouverte HAL Access content directly
Journal Articles European Journal of Paediatric Neurology Year : 2013

Elaborating the phenotypic spectrum associated with mutations in ARFGEF2: Case study and literature review

Ibrahim Tanyalçin
  • Function : Author
Helene Verhelst
  • Function : Author
Dicky J.J. Halley
  • Function : Author
Tim Vanderhasselt
  • Function : Author
Laurent Villard
Génétique Médicale et Génomique Fonctionnelle
CV
Cyril Goizet
  • Function : Author
  • PersonId : 925163
Service de génétique médicale
Willy Lissens
  • Function : Author
  • PersonId : 901068
Center for Medical Genetics
Grazia M. Mancini
  • Function : Author
Anna C. Jansen
  • Function : Author

Domains

Life Sciences [q-bio] Life Sciences [q-bio] Genetics Life Sciences [q-bio] Human health and pathology Life Sciences [q-bio] Neurons and Cognition [q-bio.NC]

Laurent Villard  : Connect in order to contact the contributor

https://hal-amu.archives-ouvertes.fr/hal-01668668

Submitted on : Wednesday, December 20, 2017-11:03:01 AM

Last modification on : Friday, March 24, 2023-2:53:06 PM

Not file

Dates and versions

hal-01668668 , version 1 (20-12-2017)

Identifiers

Cite

Ibrahim Tanyalçin, Helene Verhelst, Dicky J.J. Halley, Tim Vanderhasselt, Laurent Villard, et al.. Elaborating the phenotypic spectrum associated with mutations in ARFGEF2: Case study and literature review. European Journal of Paediatric Neurology, 2013, 17 (6), pp.666 - 670. ⟨10.1016/j.ejpn.2013.05.002⟩. ⟨hal-01668668⟩

Export

BibTeX TEI Dublin Core DC Terms EndNote Datacite

Collections

CNRS UNIV-AMU MMG
27 View
0 Download

Altmetric

Share

Gmail Facebook Twitter LinkedIn More