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A rare missense variant in theATP2C2gene is associated with..:
Martinelli, Angela
;
Rice, Mabel L
;
Talcott, Joel B
...
Human Molecular Genetics. 30 (2021) 12 - p. 1160-1171 , 2021
Link:
https://doi.org/10.1093/hmg/ddab111
RT Journal T1
A rare missense variant in theATP2C2gene is associated with language impairment and related measures
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_hmg_ddab111&Exemplar=1&LAN=DE A1 Martinelli, Angela A1 Rice, Mabel L A1 Talcott, Joel B A1 Diaz, Rebeca A1 Smith, Shelley A1 Raza, Muhammad Hashim A1 Snowling, Margaret J A1 Hulme, Charles A1 Stein, John A1 Hayiou-Thomas, Marianna E A1 Hawi, Ziarih A1 Kent, Lindsey A1 Pitt, Samantha J A1 Newbury, Dianne F A1 Paracchini, Silvia PB Oxford University Press (OUP) YR 2021 SN 0964-6906 SN 1460-2083 JF Human Molecular Genetics VO 30 IS 12 SP 1160 OP 1171 LK http://dx.doi.org/https://doi.org/10.1093/hmg/ddab111 DO https://doi.org/10.1093/hmg/ddab111 SF ELIB - SuUB Bremen
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