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Bi-allelic loss-of-function variants in BCAS3 cause a syndr..:
Hengel, Holger
;
Hannan, Shabab B
;
Dyack, Sarah
...
https://mediatum.ub.tum.de/1616867. , 2021
Link:
https://mediatum.ub.tum.de/1616867
RT Journal T1
Bi-allelic loss-of-function variants in BCAS3 cause a syndromic neurodevelopmental disorder
UL https://suche.suub.uni-bremen.de/peid=base-fttumuenchen:oai:mediatum.ub.tum.de:node_1616867&Exemplar=1&LAN=DE A1 Hengel, Holger A1 Hannan, Shabab B A1 Dyack, Sarah A1 MacKay, Sara B A1 Schatz, Ulrich A1 Fleger, Martin A1 Kurringer, Andreas A1 Balousha, Ghassan A1 Ghanim, Zaid A1 Alkuraya, Fowzan S A1 Alzaidan, Hamad A1 Alsaif, Hessa S A1 Mitani, Tadahiro A1 Bozdogan, Sevcan A1 Pehlivan, Davut A1 Lupski, James R A1 Gleeson, Joseph J A1 Dehghani, Mohammadreza A1 Mehrjardi, Mohammad Y.V A1 Sherr, Elliott H A1 Parks, Kendall C A1 Argilli, Emanuela A1 Begtrup, Amber A1 Galehdari, Hamid A1 Balousha, Osama A1 Shariati, Gholamreza A1 Mazaheri, Neda A1 Malamiri, Reza A A1 Pagnamenta, Alistair T A1 Kingston, Helen A1 Banka, Siddharth A1 Jackson, Adam A1 Osmond, Mathew A1 Rieß, Angelika A1 Haack, Tobias B A1 Nägele, Thomas A1 Schuster, Stefanie A1 Hauser, Stefan A1 Admard, Jakob A1 Casadei, Nicolas A1 Velic, Ana A1 Macek, Boris A1 Ossowski, Stephan A1 Houlden, Henry A1 Maroofian, Reza A1 Schöls, Ludger PB Elsevier BV YR 2021 K1 info:eu-repo/classification/ddc/ JF https://mediatum.ub.tum.de/1616867 LK http://dx.doi.org/https://mediatum.ub.tum.de/1616867 DO https://mediatum.ub.tum.de/1616867 SF ELIB - SuUB Bremen
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