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Bi-allelic CAMSAP1 variants cause a clinically recognizable..:
Khalaf-Nazzal, Reham
;
Fasham, James
;
Inskeep, Katherine A.
...
The American Journal of Human Genetics. 109 (2022) 11 - p. 2068-2079 , 2022
Link:
https://doi.org/10.1016/j.ajhg.2022.09.012
RT Journal T1
Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ajhg.2022.09.012&Exemplar=1&LAN=DE A1 Khalaf-Nazzal, Reham A1 Fasham, James A1 Inskeep, Katherine A. A1 Blizzard, Lauren E. A1 Leslie, Joseph S. A1 Wakeling, Matthew N. A1 Ubeyratna, Nishanka A1 Mitani, Tadahiro A1 Griffith, Jennifer L. A1 Baker, Wisam A1 Al-Hijawi, Fida' A1 Keough, Karen C. A1 Gezdirici, Alper A1 Pena, Loren A1 Spaeth, Christine G. A1 Turnpenny, Peter D. A1 Walsh, Joseph R. A1 Ray, Randall A1 Neilson, Amber A1 Kouranova, Evguenia A1 Cui, Xiaoxia A1 Curiel, David T. A1 Pehlivan, Davut A1 Akdemir, Zeynep Coban A1 Posey, Jennifer E. A1 Lupski, James R. A1 Dobyns, William B. A1 Stottmann, Rolf W. A1 Crosby, Andrew H. A1 Baple, Emma L. PB Elsevier BV YR 2022 SN 0002-9297 JF The American Journal of Human Genetics VO 109 IS 11 SP 2068 OP 2079 LK http://dx.doi.org/https://doi.org/10.1016/j.ajhg.2022.09.012 DO https://doi.org/10.1016/j.ajhg.2022.09.012 SF ELIB - SuUB Bremen
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