A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population

S. Yzer; L.I. van den Born; J. Schuil; H.Y. Kroes; X et al.

A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population

Translated title of the contribution: A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population

S. Yzer, L.I. van den Born, J. Schuil, H.Y. Kroes, X et al.

Department of Genetics

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

Translated title of the contribution	A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population
Original language	Undefined/Unknown
Pages (from-to)	709-713
Number of pages	5
Journal	Journal of Medical Genetics
Volume	40
Issue number	9
Publication status	Published - 2003

Cite this

@article{c6e6a0d89c98413494875780c54bfb46,

title = "A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population",

author = "S. Yzer and {van den Born}, L.I. and J. Schuil and H.Y. Kroes and {et al.}, X",

year = "2003",

language = "Undefined/Unknown",

volume = "40",

pages = "709--713",

journal = "Journal of Medical Genetics",

issn = "0022-2593",

publisher = "BMJ Publishing Group",

number = "9",

}

A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population. / Yzer, S.; van den Born, L.I.; Schuil, J. et al.
In: Journal of Medical Genetics, Vol. 40, No. 9, 2003, p. 709-713.

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

TY - JOUR

T1 - A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population

AU - Yzer, S.

AU - van den Born, L.I.

AU - Schuil, J.

AU - Kroes, H.Y.

AU - et al., X

PY - 2003

Y1 - 2003

M3 - Article

SN - 0022-2593

VL - 40

SP - 709

EP - 713

JO - Journal of Medical Genetics

JF - Journal of Medical Genetics

IS - 9

ER -