Sabina Liechti und Mutations - Info zur Person

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shows tRNASer(UCN) mutations in a subgroup withJournal of Medical Genetics

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von M Jaksch · · Zitiert von: 94 — Michaela Jaksch, Sabine Hofmann, Stephanie Kleinle, Sabina Liechti-Gallati,. Dieter E Pongratz, Josef Miuller-Hocker, Kerry B Jedele, Thomas Meitinger,. Klaus ...

Frequency of mitochondrial transfer RNA mutations and deletions in...

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Sabina Liechti-Gallati b, Hanns Lochmuller e, Rita Horvath a; a Metabolic Disease Centre Munich-Schwabing

Mutations in the MTM1 Gene Implicated in X-Linked ...Oxford Academic

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von J Laporte · · Zitiert von: 148 — Sabina Liechti-Gallati ,. Sabina Liechti-Gallati. 2. Department of Clinical Research, University of Berne. , Berne, Switzerland. Search for other works by ...

(PDF) Genotype/Phenotype Association in Cystic Fibrosis:Amanote Research

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Genotype/Phenotype Association in Cystic Fibrosis: Analyses of the ΔF508, R553X, and 3905insT Mutations by Sabina Liechti-Gallati, Irene Bonsall,

Association Between Haplotypes and Specific Mutations ...Amanote Research

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Association Between Haplotypes and Specific Mutations in Swiss Cystic Fibrosis Families by Sabina Liechti-Gallati, Naseem Malik, Mualla Alkan, Marco.

Association between Haplotypes and Specific Mutations in Swiss Cystic...

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Article

Alle Infos zum Namen "Sabina Liechti"

Jocelyn LAPORTEIGBMC

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Sabina Liechti-Gallati. Human Mutation ; Volume: 11 ; Page: HAL DOI Characterization of mutations in the myotubularin gene in twenty six patients ...

Regulation of MTMR2 by Phosphorylation - bac-lac.gc.cabac-lac.gc.ca

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von N Franklin · — Blondeau, Sabina Liechti-Gallati, and Jean-Louis Mandel. MTM1 Mutations in X-Linked. Myotubular Myopathy. Human Mutation. 15: (2000).