Disease
|
Mutation component
|
Alzheimers
|
Amyloid precursors
|
Fronto temporal
dementia
|
Microtubule
associated protein tau(MAPT)
|
Parkinsons disease
|
Alpha-synuclein
|
Charcot-Marie-
Tooth disease type
1A (CMT1A)
|
PMP22(duplication),hereditary
liability to pressure palsies (HNPP)(reciprocal deletion)
|
spinal muscular
atrophy
|
survival motor
neuron 2
|
Pelizaeus-Merzbacher
Syndrome
|
Proteolipid
protein 1
|
Late-onset
leukodystrophy
|
Lamin B1
|
Schizophrenia
|
Deletion at ch1q and
ch15q
|
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