CGNB3 m utations account for 50% of all cases with autosomal recessive achromatopsia

Khol; S; Varsany; B; Antunes; Ga; Baumann; B; Hoyng; Cb; Jagle; H; Rosemberg; T; Kellner; U; Lorenz; B; Salati; R; Jurklies; B; Farks; A; Andreasson; S; Weleber; Rg; Jacobson; Sg; Rudolf; G; Castellan; C; Dollfus; H; Legius; E; Anastasi M; M; Bitoun; P; Lev; D; Sieving; Pa; Munier; Fl; Zrenner; E; Sharpe; Lt; Cremers; Fpm; Wissinger; B

    Risultato della ricerca: Article

    Lingua originaleUndefined/Unknown
    pagine (da-a)302-308
    RivistaEuropean Journal of Human Genetics
    Volume13 (3)
    Stato di pubblicazionePublished - 2005

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    Khol; S; Varsany; B; Antunes; Ga; Baumann; B; Hoyng; Cb; Jagle; H; Rosemberg; T; Kellner; U; Lorenz; B; Salati; R; Jurklies; B; Farks; A; Andreasson; S; Weleber; Rg; Jacobson; Sg; Rudolf; G; Castellan; C; Dollfus; H; Legius; E; Anastasi M; M; Bitoun; P; Lev; D; Sieving; Pa; Munier; Fl; Zrenner; E; Sharpe; Lt; Cremers; Fpm; Wissinger; B (2005). CGNB3 m utations account for 50% of all cases with autosomal recessive achromatopsia. European Journal of Human Genetics, 13 (3), 302-308.

    CGNB3 m utations account for 50% of all cases with autosomal recessive achromatopsia. / Khol; S; Varsany; B; Antunes; Ga; Baumann; B; Hoyng; Cb; Jagle; H; Rosemberg; T; Kellner; U; Lorenz; B; Salati; R; Jurklies; B; Farks; A; Andreasson; S; Weleber; Rg; Jacobson; Sg; Rudolf; G; Castellan; C; Dollfus; H; Legius; E; Anastasi M; M; Bitoun; P; Lev; D; Sieving; Pa; Munier; Fl; Zrenner; E; Sharpe; Lt; Cremers; Fpm; Wissinger; B.

    In: European Journal of Human Genetics, Vol. 13 (3), 2005, pag. 302-308.

    Risultato della ricerca: Article

    Khol; S; Varsany; B; Antunes; Ga; Baumann; B; Hoyng; Cb; Jagle; H; Rosemberg; T; Kellner; U; Lorenz; B; Salati; R; Jurklies; B; Farks; A; Andreasson; S; Weleber; Rg; Jacobson; Sg; Rudolf; G; Castellan; C; Dollfus; H; Legius; E; Anastasi M; M; Bitoun; P; Lev; D; Sieving; Pa; Munier; Fl; Zrenner; E; Sharpe; Lt; Cremers; Fpm; Wissinger; B 2005, 'CGNB3 m utations account for 50% of all cases with autosomal recessive achromatopsia', European Journal of Human Genetics, vol. 13 (3), pagg. 302-308.
    Khol; S; Varsany; B; Antunes; Ga; Baumann; B; Hoyng; Cb; Jagle; H; Rosemberg; T; Kellner; U; Lorenz; B; Salati; R; Jurklies; B; Farks; A; Andreasson; S; Weleber; Rg; Jacobson; Sg; Rudolf; G; Castellan; C; Dollfus; H; Legius; E; Anastasi M; M; Bitoun; P; Lev; D; Sieving; Pa; Munier; Fl; Zrenner; E; Sharpe; Lt; Cremers; Fpm; Wissinger; B. CGNB3 m utations account for 50% of all cases with autosomal recessive achromatopsia. European Journal of Human Genetics. 2005;13 (3):302-308.
    Khol; S; Varsany; B; Antunes; Ga; Baumann; B; Hoyng; Cb; Jagle; H; Rosemberg; T; Kellner; U; Lorenz; B; Salati; R; Jurklies; B; Farks; A; Andreasson; S; Weleber; Rg; Jacobson; Sg; Rudolf; G; Castellan; C; Dollfus; H; Legius; E; Anastasi M; M; Bitoun; P; Lev; D; Sieving; Pa; Munier; Fl; Zrenner; E; Sharpe; Lt; Cremers; Fpm; Wissinger; B. / CGNB3 m utations account for 50% of all cases with autosomal recessive achromatopsia. In: European Journal of Human Genetics. 2005 ; Vol. 13 (3). pagg. 302-308.
    @article{112323d6ba2844908587973868404227,
    title = "CGNB3 m utations account for 50{\%} of all cases with autosomal recessive achromatopsia",
    author = "{Khol; S; Varsany; B; Antunes; Ga; Baumann; B; Hoyng; Cb; Jagle; H; Rosemberg; T; Kellner; U; Lorenz; B; Salati; R; Jurklies; B; Farks; A; Andreasson; S; Weleber; Rg; Jacobson; Sg; Rudolf; G; Castellan; C; Dollfus; H; Legius; E; Anastasi M; M; Bitoun; P; Lev; D; Sieving; Pa; Munier; Fl; Zrenner; E; Sharpe; Lt; Cremers; Fpm; Wissinger; B} and Mario Anastasi",
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    AU - Khol; S; Varsany; B; Antunes; Ga; Baumann; B; Hoyng; Cb; Jagle; H; Rosemberg; T; Kellner; U; Lorenz; B; Salati; R; Jurklies; B; Farks; A; Andreasson; S; Weleber; Rg; Jacobson; Sg; Rudolf; G;

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