SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein
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SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 14 August 2013
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
SETX mutations are a frequent ...... evated serum alpha-fetoprotein
@en
SETX mutations are a frequent ...... vated serum alpha-fetoprotein.
@nl
type
label
SETX mutations are a frequent ...... evated serum alpha-fetoprotein
@en
SETX mutations are a frequent ...... vated serum alpha-fetoprotein.
@nl
prefLabel
SETX mutations are a frequent ...... evated serum alpha-fetoprotein
@en
SETX mutations are a frequent ...... vated serum alpha-fetoprotein.
@nl
P2093
P2860
P50
P356
P1476
SETX mutations are a frequent ...... evated serum alpha-fetoprotein
@en
P2093
Caterina Mariotti
Davide Pareyson
Giovanna Zorzi
Lorenzo Nanetti
Simona Cavalieri
Viviana Pensato
P2860
P2888
P356
10.1186/1750-1172-8-123
P577
2013-08-14T00:00:00Z
P5875
P6179
1006187047