First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy
Copyright policy ) G C, Korenke; E, Krasemann; V, Meier; W, Beuche; D H, Hunneman; F, Hanefeld;
First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy
- LMU Klinikum Germany
- Institut für Humangenetik Germany
- University of Göttingen Germany
Family Health, Male, DNA Mutational Analysis, Mutation, Missense, Membrane Proteins, DNA, Exons, Middle Aged, ATP Binding Cassette Transporter, Subfamily D, Member 1, Deoxyribonuclease HpaII, Amino Acid Substitution, Humans, Point Mutation, ATP-Binding Cassette Transporters, Female, Adrenoleukodystrophy
Family Health, Male, DNA Mutational Analysis, Mutation, Missense, Membrane Proteins, DNA, Exons, Middle Aged, ATP Binding Cassette Transporter, Subfamily D, Member 1, Deoxyribonuclease HpaII, Amino Acid Substitution, Humans, Point Mutation, ATP-Binding Cassette Transporters, Female, Adrenoleukodystrophy
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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
Citations provided by BIP!popularityPopularity provided by BIP!
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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