Published in
Cell Press, American Journal of Human Genetics, 1(108), p. 176-185, 2021
DOI: 10.1016/j.ajhg.2020.10.017
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Missense variants in the N-terminal domain of the A isoform of FHF2/FGF13 cause an X-linked developmental and epileptic encephalopathy
Journal article published in 2020 by
Andrew E. Fry 
,
Christopher Marra,
Anna V. Derrick,
William O. Pickrell,
Adam T. Higgins,
Johann te Water Naude,
Martin A. McClatchey,
Sally J. Davies,
Kay A. Metcalfe,
Hui Jeen Tan,
Rajiv Mohanraj,
Shivaram Avula,
Denise Williams,
Lauren I. Brady,
Ronit Mesterman
and other authors.
,
Christopher Marra,
Anna V. Derrick,
William O. Pickrell,
Adam T. Higgins,
Johann te Water Naude,
Martin A. McClatchey,
Sally J. Davies,
Kay A. Metcalfe,
Hui Jeen Tan,
Rajiv Mohanraj,
Shivaram Avula,
Denise Williams,
Lauren I. Brady,
Ronit Mesterman
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
Full text: Unavailable
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