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
|
Sunday, May 19, 2013
DISEASE/CHROMOSOME
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
|
Subscribe to:
Posts (Atom)