Sunday, May 19, 2013

DISEASE/CHROMOSOME


DISEASE
CHROMOSOME/GENE INVOLVED
SCHIZOPHRENIA
DELETION AT 15q and 1q
AUTISM
DELETION AT 15q and 16p
EPILEPSY
16p DELETION
AUTISM
DUPLICATION OF X LINKED MeCP2 GENE
RETT SYNDROME
POINT MUTATION OF MeCP2 GENE


DISEASE-GENE MUTATION NEUROLOGIC DISEASES


DISEASE
GENE MUTATION
FAMILIAL ALZHEIMER’S DISEASE
AMYLOID PRECURSOR PROTEIN
FRONTO TEMPORAL DEMENTIA
MICROTUBULE ASSOCIATED PROTEIN TAU
PARKINSON’S DISEASE
ALPHA SYNEUCLEIN
CHARCOT MARIE TOOTH DISEASE TYPE 1 A
MYELIN PROTEIN PMP22
SPINAL MUSCULAR ATROPHY
SURVIVAL MOTOR NEURON2
PELIZAEUS-MERZBACHER SYNDROME(DEMYELINATING DISORDER
PROTEOLIPID PROTEIN 1
LATE ONSET LEUKODYSTROPHY
LAMININ B1