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Results: 1-4 |
Results: 4
Screening of the ryanodine receptor gene in 105 malignant hyperthermia families: novel mutations and concordance with the in vitro contracture test
Authors: Brandt, A Schleithoff, L Jurkat-Rott, K Klingler, W Baur, C Lehmann-Horn, F
Citation: A. Brandt et al., Screening of the ryanodine receptor gene in 105 malignant hyperthermia families: novel mutations and concordance with the in vitro contracture test, HUM MOL GEN, 8(11), 1999, pp. 2055-2062
Loss of wild-type MEN1 gene expression in multiple endocrine neoplasia type 1-associated parathyroid adenoma
Authors: Ludwig, L Schleithoff, L Kessler, H Wagner, PK Boehm, BO Karges, W
Citation: L. Ludwig et al., Loss of wild-type MEN1 gene expression in multiple endocrine neoplasia type 1-associated parathyroid adenoma, ENDOCR J, 46(4), 1999, pp. 539-544
Genomic structure and functional expression of a human alpha(2)/delta calcium channel subunit gene (CACNA2)
Authors: Schleithoff, L Mehrke, G Reutlinger, B Lehmann-Horn, F
Citation: L. Schleithoff et al., Genomic structure and functional expression of a human alpha(2)/delta calcium channel subunit gene (CACNA2), GENOMICS, 61(2), 1999, pp. 201-209
A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions
Authors: Lerche, H Biervert, C Alekov, AK Schleithoff, L Lindner, M Klingler, W Bretschneider, F Mitrovic, N Jurkat-Rott, K Bode, H Lehmann-Horn, F Steinlein, OK
Citation: H. Lerche et al., A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions, ANN NEUROL, 46(3), 1999, pp. 305-312
Risultati: 1-4 |