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J. Gurgel-Gianetti
J. Gurgel-Gianetti
Universidade Federal de Minas Gerais
Biology
Exon
Mutation
Genetics
Griscelli syndrome type 2
3
Papers
19
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P.4.13 Central core disease (CCD): Improving the screening for mutations in RYR1 gene
2013
Neuromuscular Disorders
T. Cuperman
S. Alcântara
Naila Cristina V. Lourenço
L.U. Yamamoto
R. Pavanello
Helga Ca Silva
J. Gurgel-Gianetti
Mayana Zatz
Acary Sb Oliveira
Mariz Vainzof
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Joining the pieces of a puzzle: The Brazilian neurolipidoses network
2011
Molecular Genetics and Metabolism
Charles Marques Lourenço
Fernando Kok
M.L.S. Santos
D. Bomfim
J. Gurgel-Gianetti
Vanessa van der Linden
Erlane Marques Ribeiro
José Simon Camelo
Janice Carneiro Coelho
Roberto Giugliani
W. Marques
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Griscelli syndrome-type 2 in twin siblings: case report and update on RAB27A human mutations and gene structure
2008
Brazilian Journal of Medical and Biological Research
I.P. Meschede
T.O. Santos
T C Izidoro-Toledo
J. Gurgel-Gianetti
Enilza M. Espreafico
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Citations (19)
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