دورية أكاديمية
GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates
| العنوان: | GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates |
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| المؤلفون: | Ouyang, QingAff1, Aff2, Aff3, Aff4, Kavanaugh, Brian C.Aff1, Aff2, Aff4, Joesch-Cohen, LenaAff2, Aff3, Aff4, Dubois, Bethany, Wu, QingAff3, Aff4, Schmidt, MichaelAff1, Aff2, Aff3, Aff4, Baytas, OzanAff1, Aff2, Aff3, Aff4, Pastore, Stephen F.Aff5, Aff6, Harripaul, RicardoAff5, Aff6, Mishra, Sasmita, Hussain, Abrar, Kim, Katherine H., Holler-Managan, Yolanda F., Ayub, Muhammad, Mir, Asif, Vincent, John B.Aff5, Aff6, Aff10, Liu, Judy S.Aff3, Aff4, Aff11, Morrow, Eric M.Aff1, Aff2, Aff3, Aff4, Aff12 |
| المصدر: | Human Genetics. 138(10):1183-1200 |
| قاعدة البيانات: | Springer Nature Journals |
Find this article in full text from Springer Verlag. 
Full Text Finder | تدمد: | 03406717 14321203 |
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| DOI: | 10.1007/s00439-019-02057-x |