Molecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areas.

BMC genetics

Volumn 8, Issue , 2007, Pages 72-

  Royer, Barbara ^a   Soares, Dinesh C ^a   Barlow, Paul N ^a   Bontrop, Ronald E ^a   Roll, Patrice ^a   Robaglia Schlupp, Andrée ^a   Blancher, Antoine ^a   Levasseur, Anthony ^a   Cau, Pierre ^a   Pontarotti, Pierre ^a   Szepetowski, Pierre ^a  

^a INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

NERVE PROTEIN; SRPX2 PROTEIN, HUMAN; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ANIMAL; ARTICLE; BRAIN DISEASE; CHEMICAL STRUCTURE; FEMALE; FRONTAL LOBE; GENETICS; HUMAN; MOLECULAR EVOLUTION; PHYLOGENY; PRIMATE; PROTEIN ANALYSIS; SEQUENCE ALIGNMENT; SINGLE NUCLEOTIDE POLYMORPHISM; SPECIES DIFFERENCE; SPEECH;

AMINO ACID SEQUENCE; ANIMALS; BRAIN DISEASES; EVOLUTION, MOLECULAR; FEMALE; FRONTAL LOBE; HUMANS; MODELS, MOLECULAR; NERVE TISSUE PROTEINS; PHYLOGENY; POLYMORPHISM, SINGLE NUCLEOTIDE; PRIMATES; PROTEIN INTERACTION MAPPING; SEQUENCE ALIGNMENT; SPECIES SPECIFICITY; SPEECH;

EID: 38449103454     PISSN: None     EISSN: 14712156     Source Type: Journal    
DOI: 10.1186/1471-2156-8-72     Document Type: Article

References (0)