Thirteen novel mutations in the NR0B1 (DAX1) gene as cause of adrenal hypoplasia congenita

N Krone; FG Riepe; R Dörr; M Morlot; K-H Rudorff; Sten Drop; Joachim Weigel; M Pura; A Kreze; M Boronat; F de Luca; A Tiulpakov; C-J Partsch; M Peter; WG Sippell

Thirteen novel mutations in the NR0B1 (DAX1) gene as cause of adrenal hypoplasia congenita

N Krone, FG Riepe, R Dörr, M Morlot, K-H Rudorff, Sten Drop, Joachim Weigel, M Pura, A Kreze, M Boronat, F de Luca, A Tiulpakov, C-J Partsch, M Peter, WG Sippell

Research output: Contribution to journal › Article › Academic › peer-review

21 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	502-503
Number of pages	2
Journal	Human Mutation
Volume	25
Publication status	Published - 2005

Cite this

@article{fb0b432eb0a6441f80ac6b3528d24b70,

title = "Thirteen novel mutations in the NR0B1 (DAX1) gene as cause of adrenal hypoplasia congenita",

author = "N Krone and FG Riepe and R D{\"o}rr and M Morlot and K-H Rudorff and Sten Drop and Joachim Weigel and M Pura and A Kreze and M Boronat and {de Luca}, F and A Tiulpakov and C-J Partsch and M Peter and WG Sippell",

year = "2005",

language = "Undefined/Unknown",

volume = "25",

pages = "502--503",

journal = "Human Mutation",

issn = "1059-7794",

publisher = "Wiley-Liss Inc.",

}

TY - JOUR

T1 - Thirteen novel mutations in the NR0B1 (DAX1) gene as cause of adrenal hypoplasia congenita

AU - Krone, N

AU - Riepe, FG

AU - Dörr, R

AU - Morlot, M

AU - Rudorff, K-H

AU - Drop, Sten

AU - Weigel, Joachim

AU - Pura, M

AU - Kreze, A

AU - Boronat, M

AU - de Luca, F

AU - Tiulpakov, A

AU - Partsch, C-J

AU - Peter, M

AU - Sippell, WG

PY - 2005

Y1 - 2005

M3 - Article

VL - 25

SP - 502

EP - 503

JO - Human Mutation

JF - Human Mutation

SN - 1059-7794

ER -