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1 Ergebnisse
1
GPT2 mutations in autosomal recessive developmental disabil..:
Ouyang, Qing
;
Kavanaugh, Brian C.
;
Joesch-Cohen, Lena
...
Human Genetics. 138 (2019) 10 - p. 1183-1200 , 2019
Link:
https://doi.org/10.1007/s00439-019-02057-x
RT Journal T1
GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates
UL https://suche.suub.uni-bremen.de/peid=cr-10.1007_s00439-019-02057-x&Exemplar=1&LAN=DE A1 Ouyang, Qing A1 Kavanaugh, Brian C. A1 Joesch-Cohen, Lena A1 Dubois, Bethany A1 Wu, Qing A1 Schmidt, Michael A1 Baytas, Ozan A1 Pastore, Stephen F. A1 Harripaul, Ricardo A1 Mishra, Sasmita A1 Hussain, Abrar A1 Kim, Katherine H. A1 Holler-Managan, Yolanda F. A1 Ayub, Muhammad A1 Mir, Asif A1 Vincent, John B. A1 Liu, Judy S. A1 Morrow, Eric M. PB Springer Science and Business Media LLC YR 2019 SN 0340-6717 SN 1432-1203 JF Human Genetics VO 138 IS 10 SP 1183 OP 1200 LK http://dx.doi.org/https://doi.org/10.1007/s00439-019-02057-x DO https://doi.org/10.1007/s00439-019-02057-x SF ELIB - SuUB Bremen
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