Human genetic disorders of axon guidance.

Cold Spring Harbor perspectives in biology

Volumn 2, Issue 3, 2010, Pages

  Engle, Elizabeth C ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LIGAND;

ANIMAL; BIOLOGICAL MODEL; BRAIN; DEVELOPMENTAL BIOLOGY; FIBROSIS; GENETIC DISORDER; GENETICS; HUMAN; KALLMANN SYNDROME; MUSCLE; MUTATION; NERVE FIBER; NEUROLOGIC DISEASE; PATHOLOGY; PHYSIOLOGY; PRENATAL DEVELOPMENT; REVIEW; SYNDROME;

ANIMALS; AXONS; BRAIN; DEVELOPMENTAL BIOLOGY; FIBROSIS; GENETIC DISEASES, INBORN; HUMANS; KALLMANN SYNDROME; LIGANDS; MODELS, BIOLOGICAL; MUSCLES; MUTATION; NERVOUS SYSTEM DISEASES; SYNDROME;

EID: 77957276921     PISSN: None     EISSN: 19430264     Source Type: Journal    
DOI: 10.1101/cshperspect.a001784     Document Type: Review

References (160)