Exclusion of chromosome regions 6p12 and 15q11, but not chromosome region 7p11, in a German family with autosomal dominant congenital nystagmus

C. Klein; P. Vieregge; W. Heide; B. Kemper; M. Hagedorn-Greiwe; J. Hagenah; C. Vollmer; X. O. Breakefield; D. Kömpf; L. Ozelius

doi:10.1006/geno.1998.5535

Exclusion of chromosome regions 6p12 and 15q11, but not chromosome region 7p11, in a German family with autosomal dominant congenital nystagmus

C. Klein, P. Vieregge, W. Heide, B. Kemper, M. Hagedorn-Greiwe, J. Hagenah, C. Vollmer, X. O. Breakefield, D. Kömpf, L. Ozelius^*

^*Korrespondierende/r Autor/-in für diese Arbeit

Harvard University

36 Zitate (Scopus)

Originalsprache	Englisch
Zeitschrift	Genomics
Jahrgang	54
Ausgabenummer	1
Seiten (von - bis)	176-177
Seitenumfang	2
ISSN	0888-7543
DOIs	https://doi.org/10.1006/geno.1998.5535
Publikationsstatus	Veröffentlicht - 15.11.1998

Fördermittel

We thank all family members for their cooperation and assistance. This work was supported by the Dystonia Medical Research Foundation (L.O., X.O.B.), NIH Grant RO1NS28384-07 (X.O.B), and the Deutsche Forschungsgemeinschaft (C.K.).

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

SDG 3 – Gesundheit und Wohlergehen
SDG 10 – Weniger Ungleichheiten

Dokumente

10.1006/geno.1998.5535

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author = "C. Klein and P. Vieregge and W. Heide and B. Kemper and M. Hagedorn-Greiwe and J. Hagenah and C. Vollmer and Breakefield, \{X. O.\} and D. K{\"o}mpf and L. Ozelius",

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AU - Klein, C.

AU - Vieregge, P.

AU - Heide, W.

AU - Kemper, B.

AU - Hagedorn-Greiwe, M.

AU - Hagenah, J.

AU - Vollmer, C.

AU - Breakefield, X. O.

AU - Kömpf, D.

AU - Ozelius, L.

PY - 1998/11/15

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JO - Genomics

JF - Genomics

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