Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresis

Developmental Brain Research

Volumn 158, Issue 1-2, 2005, Pages 66-71

  Van Der Zwaag, Bert ^a   Burbach, J Peter H ^b   Brunner, Han G ^a   Van Bokhoven, Hans ^a   Padberg, George W ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

3q21 q22; Facial paresis; Gene expression pattern analysis; Mutational analysis

Indexed keywords

AMINO ACID SUBSTITUTION; ARTICLE; CELL MOTILITY; CHROMOSOME 3Q; EMBRYO; EMBRYO DEVELOPMENT; FACIAL NERVE PARALYSIS; GENE; GENETIC DISORDER; GENETIC VARIABILITY; MOUSE; NERVE GROWTH; NONHUMAN; NUCLEOTIDE SEQUENCE; ORTHOLOGY; PATHOGENICITY; PLEXIN A1 GENE; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RHOMBENCEPHALON; RNA PROCESSING; SEQUENCE ANALYSIS;

ANIMALS; BLOTTING, SOUTHERN; BRAIN; CHROMOSOMES, HUMAN, PAIR 3; DNA; DNA MUTATIONAL ANALYSIS; EMBRYO; FACIAL PARALYSIS; FAMILY HEALTH; FEMALE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HUMANS; IN SITU HYBRIDIZATION; LINKAGE (GENETICS); MICE; MICE, INBRED C57BL; NERVE TISSUE PROTEINS; RECEPTORS, CELL SURFACE; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER; VARIATION (GENETICS);

MURINAE;

EID: 23644434396     PISSN: 01653806     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.devbrainres.2005.06.004     Document Type: Article

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