Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia

Journal article

Peer reviewed

M.A. Simpson, H. Cross, C. Proukakis, A. Pryde, R. Hershberger, Arnaud Chatonnet, M.A. Patton and A.H. Crosby

American Journal of Human Genetics, Vol.73, pp.1147-1156

2003

Abstract

ESTHER

GENETIQUE

gène

démence

hérédité

mast syndrôme

mutation génique

paraplegie

homme

url

Find in HALView

1 Record Views

Title: Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia
Creators - without role: M.A. Simpson
H. Cross
C. Proukakis
A. Pryde
R. Hershberger
Arnaud Chatonnet - Différenciation Cellulaire et Croissance
M.A. Patton
A.H. Crosby
Publication Details: American Journal of Human Genetics, Vol.73, pp.1147-1156
Identifiers: 9946474209311
Academic Unit: Université de Montpellier
Language: English
Resource Type: Journal article
Local Fields: hal-02676915