More rapid method for simultaneous measurement of tryptophan and kynurenine by HPLC
A Laich, G Neurauter, B Widner, D Fuchs - Clinical chemistry, 2002 - academic.oup.com
A Laich, G Neurauter, B Widner, D Fuchs
Clinical chemistry, 2002•academic.oup.com2. Campuzano V, Montermino L, Molto MD, Pianese L, Cossee M, Cavalcanti F, et al.
Friedreich's ataxia: autosomal recessive disease caused by an intronic triplet repeat
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chromosome 9. Nature 1988; 334: 248–50. 4. Ben Hamida M, Belal S, Sirugo G, Ben
Hamida C, Panayides K, Ionannou P, et al. Friedreich's ataxia phenotype not linked to …
Friedreich's ataxia: autosomal recessive disease caused by an intronic triplet repeat
expansion. Science 1996; 271: 1423–7. 3. Chamberlain S, Shaw J, Rowland A, Wallis J,
South S, Nakamura Y, et al. Mapping of mutation causing Friedreich's ataxia locus on
chromosome 9. Nature 1988; 334: 248–50. 4. Ben Hamida M, Belal S, Sirugo G, Ben
Hamida C, Panayides K, Ionannou P, et al. Friedreich's ataxia phenotype not linked to …
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4. Ben Hamida M, Belal S, Sirugo G, Ben Hamida C, Panayides K, Ionannou P, et al. Friedreich’s ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families. Neurology 1993; 43: 2179–83. 5. Sokol RJ. Vitamin E and neurologic deficits. Adv Pediatr 1990; 37: 119–39. 6. Tanyel MC, Mancano LD. Neurologic findings in vitamin E deficiency. Am Fam Physician 1997; 55: 197–201.
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