Thr-4-Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch family

L.I. van den Born; M.J. van Schooneveld; L.A.M.S. de Jong; F.C.C. Riemslag; P.T.V.M. de Jong; A. Gal; E.M. Bleeker-Wagemakers

Thr-4-Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch family

L.I. van den Born, M.J. van Schooneveld, L.A.M.S. de Jong, F.C.C. Riemslag, P.T.V.M. de Jong, A. Gal, E.M. Bleeker-Wagemakers

NIN

Onderzoeksoutput: Bijdrage aan wetenschappelijk tijdschrift/periodieke uitgave › Artikel › Wetenschappelijk › peer review

327 Downloads (Pure)

Originele taal-2	Engels
Pagina's (van-tot)	51-60
Tijdschrift	Ophthalmic Genetics
Volume	15
Status	Gepubliceerd - 1994

Toegang tot document

PDF

Citeer dit

@article{6faec31112b14cbbb369f3e30c516c51,

title = "Thr-4-Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch family",

author = "Born, {L.I. van den} and Schooneveld, {M.J. van} and Jong, {L.A.M.S. de} and F.C.C. Riemslag and {de Jong}, P.T.V.M. and A. Gal and E.M. Bleeker-Wagemakers",

year = "1994",

language = "English",

volume = "15",

pages = "51--60",

journal = "Ophthalmic Genetics",

issn = "1381-6810",

publisher = "Informa Healthcare",

}

Thr-4-Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch family. / Born, L.I. van den; Schooneveld, M.J. van; Jong, L.A.M.S. de et al.

In: Ophthalmic Genetics, Vol. 15, 1994, blz. 51-60.

Onderzoeksoutput: Bijdrage aan wetenschappelijk tijdschrift/periodieke uitgave › Artikel › Wetenschappelijk › peer review

TY - JOUR

T1 - Thr-4-Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch family

AU - Born, L.I. van den

AU - Schooneveld, M.J. van

AU - Jong, L.A.M.S. de

AU - Riemslag, F.C.C.

AU - de Jong, P.T.V.M.

AU - Gal, A.

AU - Bleeker-Wagemakers, E.M.

PY - 1994

Y1 - 1994

M3 - Article

SN - 1381-6810

VL - 15

SP - 51

EP - 60

JO - Ophthalmic Genetics

JF - Ophthalmic Genetics

ER -