WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations

K. Friedrich; L. Lee; D.F. Leistritz; G. Nürnberg; B. Saha; F.M. Hisama; D.K. Eyman; D. Lessel; P. Nürnberg; C. Li; M.J. Garcia-F-Villalta; C.M. Kets; J. Schmidtke; V.T. Cruz; P.C. van den Akker; J. Boak; D. Peter; G. Compoginis; K. Cefle; S. Ozturk; N. Lopez; T. van Wessel; M. Poot; P.F. Ippel; X et al.

WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations

Translated title of the contribution: WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations

K. Friedrich, L. Lee, D.F. Leistritz, G. Nürnberg, B. Saha, F.M. Hisama, D.K. Eyman, D. Lessel, P. Nürnberg, C. Li, M.J. Garcia-F-Villalta, C.M. Kets, J. Schmidtke, V.T. Cruz, P.C. van den Akker, J. Boak, D. Peter, G. Compoginis, K. Cefle, S. OzturkN. Lopez, T. van Wessel, M. Poot, P.F. Ippel, X et al.

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

Translated title of the contribution	WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations
Original language	Undefined/Unknown
Pages (from-to)	103-111
Number of pages	9
Journal	Human Genetics
Volume	128
Issue number	1
Publication status	Published - 2010

Cite this

Friedrich, K., Lee, L., Leistritz, D. F., Nürnberg, G., Saha, B., Hisama, F. M., Eyman, D. K., Lessel, D., Nürnberg, P., Li, C., Garcia-F-Villalta, M. J., Kets, C. M., Schmidtke, J., Cruz, V. T., van den Akker, P. C., Boak, J., Peter, D., Compoginis, G., Cefle, K., ... et al., X. (2010). WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations. Human Genetics, 128(1), 103-111.

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Friedrich, K, Lee, L, Leistritz, DF, Nürnberg, G, Saha, B, Hisama, FM, Eyman, DK, Lessel, D, Nürnberg, P, Li, C, Garcia-F-Villalta, MJ, Kets, CM, Schmidtke, J, Cruz, VT, van den Akker, PC, Boak, J, Peter, D, Compoginis, G, Cefle, K, Ozturk, S, Lopez, N, van Wessel, T, Poot, M, Ippel, PF & et al., X 2010, 'WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations', Human Genetics, vol. 128, no. 1, pp. 103-111.

TY - JOUR

T1 - WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations

AU - Friedrich, K.

AU - Lee, L.

AU - Leistritz, D.F.

AU - Nürnberg, G.

AU - Saha, B.

AU - Hisama, F.M.

AU - Eyman, D.K.

AU - Lessel, D.

AU - Nürnberg, P.

AU - Li, C.

AU - Garcia-F-Villalta, M.J.

AU - Kets, C.M.

AU - Schmidtke, J.

AU - Cruz, V.T.

AU - van den Akker, P.C.

AU - Boak, J.

AU - Peter, D.

AU - Compoginis, G.

AU - Cefle, K.

AU - Ozturk, S.

AU - Lopez, N.

AU - van Wessel, T.

AU - Poot, M.

AU - Ippel, P.F.

AU - et al., X

PY - 2010

Y1 - 2010

M3 - Article

SN - 0340-6717

VL - 128

SP - 103

EP - 111

JO - Human Genetics

JF - Human Genetics

IS - 1

ER -