Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion

Onur Emre Onat; Süleyman Gülsüner; Kaya Bilgüvar; A. Nazlı Başak; Haluk Topaloğlu; Meli̇ha Tan; Üner Tan; Murat Günel; Tayfun Özçelık

doi:10.1038/ejhg.2012.170

Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion

Authors: Onur Emre Onat, Süleyman Gülsüner, Kaya Bilgüvar, A. Nazlı Başak, Haluk Topaloğlu, Meli̇ha Tan, Üner Tan, Murat Günel, Tayfun Özçelık - European Journal of Human Genetics 2012 cited by 137

Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion | Litlas