Functional analysis of mutations in SLC7A9 , and genotype–phenotype correlation in non-Type I cystinuria

By Bisceglia L.  

Human Molecular Genetics, Vol. 10, Iss. 4, 2001-02 ,pp. : 305-316

Oxford University Press

Access to resources Recommend Favorite

A mouse model for cystinuria type I

By Peters T.   Thaete C.   Popp A.   Sedlmeier R.   Grosse J.   Nehls M.C.   Russ A.   Schlueter V.  

Human Molecular Genetics, Vol. 12, Iss. 17, 2003-09 ,pp. : 2109-2120

Oxford University Press

Access to resources Recommend Favorite

Aire deficient mice develop multiple features of APECED phenotype and show altered immune response

By Ramsey C.  

Human Molecular Genetics, Vol. 11, Iss. 4, 2002-02 ,pp. : 397-409

Oxford University Press

Access to resources Recommend Favorite

Hip14l -deficient mice develop neuropathological and behavioural features of Huntington disease

By Sutton Liza M.   Sanders Shaun S.   Butland Stefanie L.   Singaraja Roshni R.   Franciosi Sonia   Southwell Amber L.   Doty Crystal N.   Schmidt Mandi E.   Mui Katherine K.N.   Kovalik Vlad   Young Fiona B.   Zhang Weining   Hayden Michael R.  

Human Molecular Genetics, Vol. 22, Iss. 3, 2013-02 ,pp. : 452-465

Oxford University Press

Access to resources Recommend Favorite

Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice

By Johnson Eric B.  

Human Molecular Genetics, Vol. 14, Iss. 22, 2005-11 ,pp. : 3523-3538

Oxford University Press

Access to resources Recommend Favorite