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Title Issue Date
Thirteen novel mutations in theNR0B1(DAX1) gene as cause of adrenal hypoplasia congenita Krone, Nils; Riepe, Felix Günther; Dörr, Helmuth-Günther; Morlot, Michel; Rudorff, Karl-Heinz, et al Issued date: 2005 DOI: 10.1002/humu.9331 Source: Human Mutation [ISSN 1059-7794], v. 25 (5), p. 502-502 JCR: 7,923 - Q1 SCIE Artículo
Genetic and cellular studies of oxidative stress in methylmalonic aciduria (MMA) cobalamin deficiency type C (cblC) with homocystinuria (MMACHC) Richard, Eva; Jorge-Finnigan, Ana; Garcia-Villoria, Judit; Merinero, Begoña; Desviat, Lourdes R., et al Issued date: 2009 DOI: 10.1002/humu.21107 Source: Human Mutation[ISSN 1059-7794],v. 30, p. 1558-1566 (Septiembre 2009) JCR: 6,887 - Q1 SCIE Artículo

Krone, Nils; Riepe, Felix Günther; Dörr, Helmuth-Günther; Morlot, Michel; Rudorff, Karl-Heinz, et al

Issued date: 2005

DOI: 10.1002/humu.9331

Source: Human Mutation [ISSN 1059-7794], v. 25 (5), p. 502-502

JCR: 7,923

- Q1

SCIE

Artículo

Richard, Eva; Jorge-Finnigan, Ana; Garcia-Villoria, Judit; Merinero, Begoña; Desviat, Lourdes R., et al

Issued date: 2009

DOI: 10.1002/humu.21107

Source: Human Mutation[ISSN 1059-7794],v. 30, p. 1558-1566 (Septiembre 2009)

JCR: 6,887

- Q1

SCIE

Artículo