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Broadening the phenotype of LRRK1 mutations - Features of m..:
Chorin, Odelia
;
Chowers, Guy
;
Agbariah, Rawan
...
European Journal of Medical Genetics. 65 (2022) 1 - p. 104383 , 2022
Link:
https://doi.org/10.1016/j.ejmg.2021.104383
RT Journal T1
Broadening the phenotype of LRRK1 mutations - Features of malignant osteopetrosis and optic nerve atrophy with intrafamilial variable expressivity
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ejmg.2021.104383&Exemplar=1&LAN=DE A1 Chorin, Odelia A1 Chowers, Guy A1 Agbariah, Rawan A1 Karklinsky, Shani A1 Barel, Ortal A1 Bar-Joseph, Ifat A1 Reznik-Wolf, Haike A1 Shamash, Jana A1 Pode-Shakked, Ben A1 Jacobson, Jeffrey M. A1 Huna-Baron, Ruth A1 Redler, Yael A1 Tirosh, Irit A1 Vivante, Asaf A1 Raas-Rothschild, Annick PB Elsevier BV YR 2022 SN 1769-7212 JF European Journal of Medical Genetics VO 65 IS 1 SP 104383 LK http://dx.doi.org/https://doi.org/10.1016/j.ejmg.2021.104383 DO https://doi.org/10.1016/j.ejmg.2021.104383 SF ELIB - SuUB Bremen
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