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Mutations in SCNM1 cause orofaciodigital syndrome due to mi..:
Iturrate, Asier
;
Rivera-Barahona, Ana
;
Flores, Carmen-Lisset
...
The American Journal of Human Genetics. 109 (2022) 10 - p. 1828-1849 , 2022
Link:
https://doi.org/10.1016/j.ajhg.2022.08.009
RT Journal T1
Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ajhg.2022.08.009&Exemplar=1&LAN=DE A1 Iturrate, Asier A1 Rivera-Barahona, Ana A1 Flores, Carmen-Lisset A1 Otaify, Ghada A. A1 Elhossini, Rasha A1 Perez-Sanz, Marina L. A1 Nevado, Julián A1 Tenorio-Castano, Jair A1 Triviño, Juan Carlos A1 Garcia-Gonzalo, Francesc R. A1 Piceci-Sparascio, Francesca A1 De Luca, Alessandro A1 Martínez, Leopoldo A1 Kalaycı, Tugba A1 Lapunzina, Pablo A1 Altunoglu, Umut A1 Aglan, Mona A1 Abdalla, Ebtesam A1 Ruiz-Perez, Victor L. PB Elsevier BV YR 2022 SN 0002-9297 JF The American Journal of Human Genetics VO 109 IS 10 SP 1828 OP 1849 LK http://dx.doi.org/https://doi.org/10.1016/j.ajhg.2022.08.009 DO https://doi.org/10.1016/j.ajhg.2022.08.009 SF ELIB - SuUB Bremen
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