Literature citations
Germline de novo mutations in GNB1 cause severe neurodevelopmental disability, hypotonia, and seizures.
Petrovski S.; Kuery S.; Myers C.T.; Anyane-Yeboa K.; Cogne B.; Bialer M.; Xia F.; Hemati P.; Riviello J.; Mehaffey M.; Besnard T.; Becraft E.; Wadley A.; Politi A.R.; Colombo S.; Zhu X.; Ren Z.; Andrews I.; Dudding-Byth T.; Schneider A.L.; Wallace G.; Rosen A.B.; Schelley S.; Enns G.M.; Corre P.; Dalton J.; Mercier S.; Latypova X.; Schmitt S.; Guzman E.; Moore C.; Bier L.; Heinzen E.L.; Karachunski P.; Shur N.; Grebe T.; Basinger A.; Nguyen J.M.; Bezieau S.; Wierenga K.; Bernstein J.A.; Scheffer I.E.; Rosenfeld J.A.; Mefford H.C.; Isidor B.; Goldstein D.B.;
Am. J. Hum. Genet. 98:1001-1010(2016)
Cited for: INVOLVEMENT IN MRD42; VARIANTS MRD42 GLU-76; GLY-76; SER-77; ARG-78; ASN-80; THR-80; PRO-95; VAL-101 AND THR-326;
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