A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts

S. Cingoz; R.B. van der Luijt; E. Kurt; M. Apaydin; I. Akkol; M.H. Ozgen

doi:10.1007/s10689-012-9586-7

A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts

Translated title of the contribution: A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts

S. Cingoz
, R.B. van der Luijt
, E. Kurt
, M. Apaydin
, I. Akkol
, M.H. Ozgen

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

Translated title of the contribution	A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts
Original language	Undefined/Unknown
Pages (from-to)	111-117
Number of pages	7
Journal	Familial Cancer
Volume	12
Issue number	1
DOIs	https://doi.org/10.1007/s10689-012-9586-7
Publication status	Published - 2013

Access to Document

10.1007/s10689-012-9586-7

http://www.ncbi.nlm.nih.gov/pubmed/?term=23224817

Cite this

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title = "A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts",

author = "S. Cingoz and \{van der Luijt\}, R.B. and E. Kurt and M. Apaydin and I. Akkol and M.H. Ozgen",

year = "2013",

doi = "10.1007/s10689-012-9586-7",

language = "Undefined/Unknown",

volume = "12",

pages = "111--117",

journal = "Familial Cancer",

issn = "1389-9600",

publisher = "Springer Science and Business Media B.V.",

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T1 - A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts

AU - Cingoz, S.

AU - van der Luijt, R.B.

AU - Kurt, E.

AU - Apaydin, M.

AU - Akkol, I.

AU - Ozgen, M.H.

PY - 2013

Y1 - 2013

U2 - 10.1007/s10689-012-9586-7

DO - 10.1007/s10689-012-9586-7

M3 - Article

C2 - 23224817

SN - 1389-9600

VL - 12

SP - 111

EP - 117

JO - Familial Cancer

JF - Familial Cancer

IS - 1

ER -