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Results: 1-6 |
Results: 6

Authors: LUDECKE B KNAPPSKOG PM CLAYTON PT SURTEES RAH CLELLAND JD HEALES SJR BRAND MP BARTHOLOME K FLATMARK T
Citation: B. Ludecke et al., RECESSIVELY INHERITED L-DOPA-RESPONSIVE PARKINSONISM IN INFANCY CAUSED BY A POINT MUTATION (L205P) IN THE TYROSINE-HYDROXYLASE GENE, Human molecular genetics, 5(7), 1996, pp. 1023-1028

Authors: WEVERS RA DERIJKVANANDEL JF GABREELS FJM LUDECKE B BLAU N BARTHOLOME K
Citation: Ra. Wevers et al., A NEW CASE OF TYROSINE-HYDROXYLASE DEFICIENCY, Journal of neurochemistry, 66, 1996, pp. 27-27

Authors: KNAPPSKOG PM FLATMARK T MALLET J LUDECKE B BARTHOLOME K
Citation: Pm. Knappskog et al., RECESSIVELY INHERITED L-DOPA-RESPONSIVE DYSTONIA CAUSED BY A POINT MUTATION (Q381K) IN THE TYROSINE-HYDROXYLASE GENE, Human molecular genetics, 4(7), 1995, pp. 1209-1212

Authors: LUDECKE B BARTHOLOME K
Citation: B. Ludecke et K. Bartholome, FREQUENT SEQUENCE VARIANT IN THE HUMAN TYROSINE-HYDROXYLASE GENE, Human genetics, 95(6), 1995, pp. 716-716

Authors: LUDECKE B DWORNICZAK B BARTHOLOME K
Citation: B. Ludecke et al., A POINT MUTATION IN THE TYROSINE-HYDROXYLASE GENE ASSOCIATED WITH SEGAWAS SYNDROME, Human genetics, 95(1), 1995, pp. 123-125

Authors: BARTHOLOME K DWORNICZAK B LUDECKE B
Citation: K. Bartholome et al., LINKAGE OF THE TYROSINE-HYDROXYLASE GENE AND SEGAWAS SYNDROME, American journal of human genetics, 53(3), 1993, pp. 889-889
Risultati: 1-6 |