New variant in exon 3 of the proteolipid protein (PLP) gene in a family with pelizaeus‐merzbacher disease
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Abstract
References (8)
Mutation of the proteolipid protein gene PLP in a human X chromosome-linked myelin disorder.
1989 • 205 citations
Individual exons encode the integral membrane domains of human myelin proteolipid protein.
1986 • 177 citations
Pelizaeus-Merzbacher disease: an X-linked neurologic disorder of myelin metabolism with a novel mutation in the gene encoding proteolipid protein.
1989 • 157 citations
Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher disease.
1991 • 152 citations
Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant.
1989 • 118 citations
Pelizaeus-Merzbacher disease: a valine to phenylalanine point mutation in a putative extracellular loop of myelin proteolipid.
1991 • 66 citations
A new mutation in the proteolipid protein (PLP) gene in a German family with pelizaeus‐merzbacher disease
1991 • 41 citations
Ahallpolymorphism in human X-linked proteolipid protein gene (PLP)
1991 • 21 citations
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