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PMP22 FRAMESHIFT MUTATION AND HEREDITARY NEUROPATHY WITH LIABILITY TOPRESSURE PALSIES - REPLY
Authors: YOUNG P WIEBUSCH H STOGBAUER F RINGELSTEIN B ASSMANN G FUNKE H
Citation: P. Young et al., PMP22 FRAMESHIFT MUTATION AND HEREDITARY NEUROPATHY WITH LIABILITY TOPRESSURE PALSIES - REPLY, Neurology, 49(5), 1997, pp. 1478-1479
A NOVEL FRAMESHIFT MUTATION IN PMP22 ACCOUNTS FOR HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES
Authors: YOUNG P WIEBUSCH H STOGBAUER F RINGELSTEIN B ASSMANN G FUNKE H
Citation: P. Young et al., A NOVEL FRAMESHIFT MUTATION IN PMP22 ACCOUNTS FOR HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES, Neurology, 48(2), 1997, pp. 450-452
4 FREQUENTLY OBSERVED POLYMORPHISMS IN THE 3'-UTR OF HUMAN PERIPHERALMYELIN PROTEIN-22 (PMP22) - IDENTIFICATION OF DIFFERENT HAPLOTYPES
Authors: YOUNG P WIEBUSCH H STOGBAUER F RINGELSTEIN B ASSMANN G FUNKE H
Citation: P. Young et al., 4 FREQUENTLY OBSERVED POLYMORPHISMS IN THE 3'-UTR OF HUMAN PERIPHERALMYELIN PROTEIN-22 (PMP22) - IDENTIFICATION OF DIFFERENT HAPLOTYPES, Clinical genetics, 49(6), 1996, pp. 321-322
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