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STROM TM
NYAKATURA G
APFELSTEDTSYLLA E
HELLEBRAND H
LORENZ B
WEBER BHF
WUTZ K
GUTWILLINGER N
RUTHER K
DRESCHER B
SAUER C
ZRENNER E
MEITINGER T
ROSENTHAL A
MEINDL A
Citation: Tm. Strom et al., AN L-TYPE CALCIUM-CHANNEL GENE MUTATED IN INCOMPLETE X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS, Nature genetics, 19(3), 1998, pp. 260-263
Authors:
RUTHER K
EHLICH P
PHILIPP A
ECKSTEIN A
ZRENNER E
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Authors:
VANDENHURK JAJM
SCHWARTZ M
VANBOKHOVEN H
VANDEPOL TJR
BOGERD L
PINCKERS AJLG
BLEEKERWAGEMAKERS EM
PAWLOWITZKI IH
RUTHER K
ROPERS HH
CREMERS FPM
Citation: Jajm. Vandenhurk et al., MOLECULAR-BASIS OF CHOROIDEREMIA (CHM) - MUTATIONS INVOLVING THE RAB ESCORT PROTEIN-1 (REP-1) GENE, Human mutation, 9(2), 1997, pp. 110-117
Authors:
VANDENHURK JAJM
HENDRIKS W
VANDEPOL DJR
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JAISSLE G
RUTHER K
KOHLER K
HARTMANN J
ZRENNER E
VANBOKHOVEN H
WIERINGA B
ROPERS HH
CREMERS FPM
Citation: Jajm. Vandenhurk et al., MOUSE CHOROIDEREMIA GENE MUTATION CAUSES PHOTORECEPTOR CELL DEGENERATION AND IS NOT TRANSMITTED THROUGH THE FEMALE GERMLINE, Human molecular genetics, 6(6), 1997, pp. 851-858
Authors:
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RUTHER K
APFELSTEDTSYLLA E
SCHLOTE W
WOHLRAB M
ZRENNER E
Citation: M. Seelinger et al., DIAGNOSTIC PROCEDURES AND OPHTHALMOLOGIC FINDINGS IN JUVENILE NEURONAL CEROID-LIPOFUSCINOSIS (BATTEN-MAYOU), Der Ophthalmologe, 94(8), 1997, pp. 557-562
Authors:
CREMERS FPM
VANDENHURK JAJM
HENDRIKS W
VANDEPOL TJR
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JAISSLE G
KOHLER K
RUTHER K
HARTMANN J
ZRENNER E
WIERINGA B
ROPERS HH
Citation: Fpm. Cremers et al., THE CHOROIDEREMIA MUTATION RESULTS IN PHOTORECEPTOR CELL DEGENERATIONIN CHIMERIC MICE BUT IS EMBRYONIC LETHAL IN HEMIZYGOTIC MICE, The FASEB journal, 11(9), 1997, pp. 798-798
Authors:
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ECKSTEIN A
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WEDEMANN H
RUTHER K
ZRENNER E
Citation: S. Kremmer et al., OCULAR FINDINGS IN PATIENTS WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA AND CYS110PHE, ARG135GLY, AND GLN344STOP MUTATIONS OF RHODOPSIN, Graefe's archive for clinical and experimental ophthalmology, 235(9), 1997, pp. 575-583
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BAATZ H
RUTHER K
PLEYER U
HARTMANN C
Citation: B. Tonnessen et al., HEMODYNAMIC AND ELECTROPHYSIOLOGICAL PARAMETERS IN INTRAVITAL MICROSCOPY OF IRIS VESSELS, Investigative ophthalmology & visual science, 38(4), 1997, pp. 4903-4903
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Citation: J. Bortlisz et al., DETERMINATION OF LOW WATER CONTENTS IN DR IED SLUDGE WITH THE HELP OFFISCHER,KARL TITRATION, Acta hydrochimica et hydrobiologica, 23(3), 1995, pp. 104-110
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THEISCHEN M
RUTHER K
WEDEMANN H
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ZRENNER E
Citation: E. Apfelstedtsylla et al., EXTENSIVE INTRAFAMILIAL AND INTERFAMILIAL PHENOTYPIC VARIATION AMONG PATIENTS WITH AUTOSOMAL-DOMINANT RETINAL DYSTROPHY AND MUTATIONS IN THE HUMAN RDS PERIPHERIN GENE, British journal of ophthalmology, 79(1), 1995, pp. 28-34
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Citation: J. Vandenhurk et al., MATERNAL TRANSMISSION OF A CHOROIDEREMIA MUTATION IN MICE IS EMBRYONIC LETHAL, American journal of human genetics, 57(4), 1995, pp. 274-274
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SCHWARTZ M
ANDREASSON S
VANDENHURK JAJM
BOGERD L
JAY M
RUTHER K
JAY B
PAWLOWITZKI IH
SANKILA EM
WRIGHT A
ROPERS HH
ROSENBERG T
CREMERS FPM
Citation: H. Vanbokhoven et al., MUTATION SPECTRUM IN THE CHM GENE OF DANISH AND SWEDISH CHOROIDEREMIAPATIENTS, Human molecular genetics, 3(7), 1994, pp. 1047-1051
Citation: A. Eckstein et al., ELECTRORETINOGRAPHIC INVESTIGATION OF UNA NESTHETIZED YOUNG-CHILDREN, Klinische Monatsblatter fur Augenheilkunde, 204(2), 1994, pp. 105-110
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Citation: G. Dewald et al., A COMMON SER THR POLYMORPHISM IN THE PERFORIN HOMOLOGOUS REGION OF HUMAN-COMPLEMENT COMPONENT C7/, Human heredity, 44(6), 1994, pp. 301-304
Authors:
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KUNISCH M
HORN M
RUTHER K
GERDING H
GAL A
ZRENNER E
Citation: E. Apfelstedtsylla et al., OCULAR FINDINGS IN A FAMILY WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA AND A FRAMESHIFT MUTATION ALTERING THE CARBOXYL-TERMINAL SEQUENCE OF RHODOPSIN, British journal of ophthalmology, 77(8), 1993, pp. 495-501
Authors:
APFELSTEDTSYLLA E
HORN M
KUNISCH M
RUTHER K
GERDING H
GAL A
ZRENNER E
Citation: E. Apfelstedtsylla et al., CLINICAL CHARACTERISTICS OF AUTOSOMAL DOMINANT RETINITIS-PIGMENTOSA (ADRP) WITH A DELETION OF 8 BASE-PAIRS AND SHIFT OF THE READING FRAME IN EXON 5 OF THE RHODOPSIN GENE, Investigative ophthalmology & visual science, 33(4), 1992, pp. 1095-1095