Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients.

R.G. van Eijsden; M. Gerards; L.M. Eijssen; A.T. Hendrickx; R.J. Jongbloed; J.H.J. Wokke; R.Q. Hintzen; M.E. Rubio-Gozalbo; I.F. Coo; E. Briem; V. Tiranti; H.J. Smeets

Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients.

Translated title of the contribution: Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients.

R.G. van Eijsden
, M. Gerards
, L.M. Eijssen
, A.T. Hendrickx
, R.J. Jongbloed
, J.H.J. Wokke
, R.Q. Hintzen
, M.E. Rubio-Gozalbo
, I.F. Coo
, E. Briem
, V. Tiranti
, H.J. Smeets

Neurology & Neurosurgery

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

Translated title of the contribution	Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients.
Original language	Undefined/Unknown
Pages (from-to)	620-627
Number of pages	8
Journal	Genetics in Medicine
Volume	8
Issue number	10
Publication status	Published - 2006

Cite this

@article{83e6852a8ceb46f7962000ce3aa33e48,

title = "Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients.",

author = "\{van Eijsden\}, R.G. and M. Gerards and L.M. Eijssen and A.T. Hendrickx and R.J. Jongbloed and J.H.J. Wokke and R.Q. Hintzen and M.E. Rubio-Gozalbo and I.F. Coo and E. Briem and V. Tiranti and H.J. Smeets",

year = "2006",

language = "Undefined/Unknown",

volume = "8",

pages = "620--627",

journal = "Genetics in Medicine",

issn = "1098-3600",

publisher = "Elsevier",

number = "10",

}

TY - JOUR

T1 - Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients.

AU - van Eijsden, R.G.

AU - Gerards, M.

AU - Eijssen, L.M.

AU - Hendrickx, A.T.

AU - Jongbloed, R.J.

AU - Wokke, J.H.J.

AU - Hintzen, R.Q.

AU - Rubio-Gozalbo, M.E.

AU - Coo, I.F.

AU - Briem, E.

AU - Tiranti, V.

AU - Smeets, H.J.

PY - 2006

Y1 - 2006

M3 - Article

SN - 1098-3600

VL - 8

SP - 620

EP - 627

JO - Genetics in Medicine

JF - Genetics in Medicine

IS - 10

ER -