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Bi-allelic loss-of-function variants in KIF21A cause severe..:

Falb, Ruth J ; Müller, Amelie J ; Klein, Wolfram...
https://jmg.bmj.com/highwire/filestream/183711/field_highwire_adjunct_files/0/jmedgenet-2021-108064supp001_data_supplement.pdf. , 2022

Link: https://doi.org/10.18725/OPARU-45991

RT Journal
T1 <Title>Bi-allelic loss-of-function variants in KIF21A cause severe fetal akinesia with arthrogryposis multiplex</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftunivulm:oai:oparu.uni-ulm.de:123456789_46067&Exemplar=1&LAN=DE
				
A1 Falb, Ruth J
A1 Müller, Amelie J
A1 Klein, Wolfram
A1 Grimmel, Mona
A1 Grasshoff, Ute
A1 Spranger, Stephanie
A1 Stöbe, Petra
A1 Gauck, Darja
A1 Kuechler, Alma
A1 Dikow, Nicola
A1 Schwaibold, Eva M C
A1 Schmidt, Christoph
A1 Averdunk, Luisa
A1 Buchert, Rebecca
A1 Heinrich, Tilman
A1 Prodan, Natalia
A1 Park, Joohyun
A1 Kehrer, Martin
A1 Sturm, Marc
A1 Kelemen, Olga
A1 Hartmann, Silke
A1 Horn, Denise
A1 Emmerich, Dirk
A1 Hirt, Nina
A1 Neumann, Armin
A1 Kristiansen, Glen
A1 Gembruch, Ulrich
A1 Haen, Susanne
A1 Siebert, Reiner
A1 Hentze, Sabine
A1 Hoopmann, Markus
A1 Ossowski, Stephan
A1 Waldmüller, Stephan
A1 Beck-Wödl, Stefanie
A1 Gläser, Dieter
A1 Tekesin, Ismail
A1 Distelmaier, Felix
A1 Riess, Olaf
A1 Kagan, Karl-Oliver
A1 Dufke, Andreas
A1 Haack, Tobias B
PB Universität Ulm
YR 2022
K1 DDC 570 / Life sciences
K1 DDC 610 / Medicine & health
K1 Nervous system diseases
K1 Genetics
K1 Neuromuscular diseases
K1 Neuropathologie
K1 Neuromuskuläre Krankheit
K1 Genetik
JF https://jmg.bmj.com/highwire/filestream/183711/field_highwire_adjunct_files/0/jmedgenet-2021-108064supp001_data_supplement.pdf
LK http://dx.doi.org/https://doi.org/10.18725/OPARU-45991
DO https://doi.org/10.18725/OPARU-45991
SF ELIB - SuUB Bremen

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