Diversity of the basic defect of homozygous CFTR mutation genotypes in humans.

F. Stanke; M. Ballmann; I. Bronsveld; T. Dörk; S. Gallati; U. Laabs; N. Derichs; M. Ritzka; H-G. Posselt; H.K. Harms; M. Griese; H. Blau; G. Mastella; J. Bijman; H. Veeze; B. Tummler

Diversity of the basic defect of homozygous CFTR mutation genotypes in humans.

Translated title of the contribution: Diversity of the basic defect of homozygous CFTR mutation genotypes in humans.

F. Stanke, M. Ballmann, I. Bronsveld, T. Dörk, S. Gallati, U. Laabs, N. Derichs, M. Ritzka, H-G. Posselt, H.K. Harms, M. Griese, H. Blau, G. Mastella, J. Bijman, H. Veeze, B. Tummler

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

Translated title of the contribution	Diversity of the basic defect of homozygous CFTR mutation genotypes in humans.
Original language	Undefined/Unknown
Pages (from-to)	47-54
Number of pages	8
Journal	Journal of Medical Genetics
Volume	45
Issue number	1
Publication status	Published - 2008

Cite this

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title = "Diversity of the basic defect of homozygous CFTR mutation genotypes in humans.",

author = "F. Stanke and M. Ballmann and I. Bronsveld and T. D{\"o}rk and S. Gallati and U. Laabs and N. Derichs and M. Ritzka and H-G. Posselt and H.K. Harms and M. Griese and H. Blau and G. Mastella and J. Bijman and H. Veeze and B. Tummler",

year = "2008",

language = "Undefined/Unknown",

volume = "45",

pages = "47--54",

journal = "Journal of Medical Genetics",

issn = "0022-2593",

publisher = "BMJ Publishing Group",

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TY - JOUR

T1 - Diversity of the basic defect of homozygous CFTR mutation genotypes in humans.

AU - Stanke, F.

AU - Ballmann, M.

AU - Bronsveld, I.

AU - Dörk, T.

AU - Gallati, S.

AU - Laabs, U.

AU - Derichs, N.

AU - Ritzka, M.

AU - Posselt, H-G.

AU - Harms, H.K.

AU - Griese, M.

AU - Blau, H.

AU - Mastella, G.

AU - Bijman, J.

AU - Veeze, H.

AU - Tummler, B.

PY - 2008

Y1 - 2008

M3 - Article

SN - 0022-2593

VL - 45

SP - 47

EP - 54

JO - Journal of Medical Genetics

JF - Journal of Medical Genetics

IS - 1

ER -