A Point Mutation at the X-Chromosomal Proteolipid Protein Locus in Pelizaeus-Merzbacher Disease Leads to Disruption of Myelinogenesis
about
Ludwig Merzbacher (1875-1942): the man behind the disease.Hereditary Lewy-body parkinsonism and evidence for a genetic etiology of Parkinson's disease.The structure and function of central nervous system myelin.A cellular mechanism governing the severity of Pelizaeus-Merzbacher disease.Many naturally occurring mutations of myelin proteolipid protein impair its intracellular transport.
P2860
A Point Mutation at the X-Chromosomal Proteolipid Protein Locus in Pelizaeus-Merzbacher Disease Leads to Disruption of Myelinogenesis
description
wetenschappelijk artikel
@nl
наукова стаття, опублікована в січні 1990
@uk
name
A Point Mutation at the X-Chro ...... o Disruption of Myelinogenesis
@en
A Point Mutation at the X-Chro ...... o Disruption of Myelinogenesis
@nl
type
label
A Point Mutation at the X-Chro ...... o Disruption of Myelinogenesis
@en
A Point Mutation at the X-Chro ...... o Disruption of Myelinogenesis
@nl
prefLabel
A Point Mutation at the X-Chro ...... o Disruption of Myelinogenesis
@en
A Point Mutation at the X-Chro ...... o Disruption of Myelinogenesis
@nl
P2093
P2860
P1476
A Point Mutation at the X-Chro ...... o Disruption of Myelinogenesis
@en
P2093
Eugen BOLTSHAUSER
Tobias DICK
Wilhelm STOFFEL
P2860
P304
P356
10.1515/BCHM3.1990.371.2.1175
P577
1990-01-01T00:00:00Z