Concepedia

V. Volpinl

VV

Statistics

Publications

2

Citations

115

H-Index

2

Active since

1993

Affiliations

Duran i Reynals Hospital(Current)

V. Volpinl is an author at Duran i Reynals Hospital specializing in genetics, genetic disorders, and human genetics.

Publications per year

1993–1993

2

Publications

2

Presymptomatic analysis of spinocerebellar ataxia type 1 (SCA1) via the expansion of the <i>SCA1</i> CAG-repeat in a large pedigree displaying anticipation and parental male bias

T. Matilla, V. Volpinl, D. E. Genis et al. · Human Molecular Genetics · 1993 · 84 citations

, , +15

Identification of two new missense mutations (K58N and R121Q) in the Norrie disease <i>(ND)</i> gene in two Spanish families

J.–J. Fuentes, V. Volpinl, F. Fernandez-Toral et al. · Human Molecular Genetics · 1993 · 31 citations

, , +10

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