Functional Consequences of PRODH Missense Mutations
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference67 articles.
1. The schizophrenia phenotype in 22q11 deletion syndrome;Bassett;Am J Psychiatry,2003
2. Biochemistry;Berg,2002
3. Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata;Braverman;Nat Genet,1997
4. The role of system A for neutral amino acid transport in the regulation of cell volume;Bussolati;Mol Membr Biol,2001
5. Characterization of single-nucleotide polymorphisms in coding regions of human genes;Cargill;Nat Genet,1999
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