Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination (Q55670897)
article by L E Warner et al published September 1996 in Neuron
Language:
Current Data About Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination
(P31) (Q13442814)

(P50) (Q2247235)
(P1545) 13
(P1932) C Van Broeckhoven

(P304) 451-60

(P407) (Q1860)

(P433) 3

(P478) 17

(P577) +1996-09-00T00:00:00Z

(P1433) (Q3338676)

(P1476) "Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination" (language: en)

(P2093) L E Warner
(P1545) 1

M J Hilz
(P1545) 2

S H Appel
(P1545) 3

J M Killian
(P1545) 4

E H Kolodry
(P1545) 5

G Karpati
(P1545) 6

S Carpenter
(P1545) 7

G V Watters
(P1545) 8

C Wheeler
(P1545) 9

D Witt
(P1545) 10

A Bodell
(P1545) 11

E Nelis
(P1545) 12

J R Lupski
(P1545) 14

other details
description article by L E Warner et al published September 1996 in Neuron

External Links
(P698) 8816708