A novel mutation (K317M) in the <i>MAPT</i> gene causes FTDP and motor neuron disease - Concepedia

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A novel mutation (K317M) in the <i>MAPT</i> gene causes FTDP and motor neuron disease

100

Citations

38

References

2005

Year

J.J. Zarranz, Isidró Ferrer, E. Lezcano, Maribel Forcadas, B. Eizaguirre, Begoña Atarés, Berta Puig, Juan Carlos Gómez‐Esteban, Covadonga Fernández-Maiztegui, I. Rouco,

Abstract

Genetic analysis revealed the same novel mutation (K317M) in exon 11 of the MAPT gene in both pedigrees. A common haplotype between members of the two pedigrees suggests that they belong to the same family.

References

	Year	Citations

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