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Inherited Peripheral Neuropathies Mutation Database
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IPN Mutations
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Table Legend
last updated 17-Feb-11
Select one of the following phenotypes:
ACCPN (AS)
ALS4
CCFDN
CH
CIDP
CMT1
CMT1/2
CMT1X
CMT2
CMT4
CMTX
dHMN
dHMN II
dHMN V
dHMN VI
dHMN with vocal fold paralysis
DSS
dysmorphic features
focally folded myelin
GAN
HMSN-L
HNA
HNPP
HS(A)N
HS(A)N I
HS(A)N II
HS(A)N III
HS(A)N IV
HS(A)N V
HSN with spastic paraplegia
peripheral neuropathy and additional features
polymorphism
Severe infantile neuropathy with diaphragmatic weakness
Silver syndrome (SPG17)
slowed NCV
test
ulceromutilating neuropathy
unknown
unspecified CMT
Select the output type:
Table Output
Detailed Output
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