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260 related items for PubMed ID: 15180699
1. Molecular analysis of GAA repeats and four linked bi-allelic markers in and around the frataxin gene in patients and normal populations from India. Chattopadhyay B, Gupta S, Gangopadhyay PK, Das SK, Roy T, Mukherjee SC, Sinha KK, Singhal BS, Bhattacharyya NP. Ann Hum Genet; 2004 May; 68(Pt 3):189-95. PubMed ID: 15180699 [Abstract] [Full Text] [Related]
2. GAA repeat polymorphism in Turkish Friedreich's ataxia patients. Yilmaz MB, Koç AF, Kasap H, Güzel AI, Sarica Y, Süleymanova D. Int J Neurosci; 2006 May; 116(5):565-74. PubMed ID: 16644517 [Abstract] [Full Text] [Related]
3. Friedreich ataxia: Detection of GAA repeat expansions and frataxin point mutations. Pandolfo M. Methods Mol Med; 2006 May; 126():197-216. PubMed ID: 16930014 [Abstract] [Full Text] [Related]
4. North and South Indian populations share a common ancestral origin of Friedreich's ataxia but vary in age of GAA repeat expansion. Singh I, Faruq M, Mukherjee O, Jain S, Pal PK, Srivastav MV, Behari M, Srivastava AK, Mukerji M. Ann Hum Genet; 2010 May; 74(3):202-10. PubMed ID: 20374234 [Abstract] [Full Text] [Related]
9. Novel, complex interruptions of the GAA repeat in small, expanded alleles of two affected siblings with late-onset Friedreich ataxia. Stolle CA, Frackelton EC, McCallum J, Farmer JM, Tsou A, Wilson RB, Lynch DR. Mov Disord; 2008 Jul 15; 23(9):1303-6. PubMed ID: 18464277 [Abstract] [Full Text] [Related]
11. Friedreich's ataxia with chorea and myoclonus caused by a compound heterozygosity for a novel deletion and the trinucleotide GAA expansion. Zhu D, Burke C, Leslie A, Nicholson GA. Mov Disord; 2002 May 15; 17(3):585-9. PubMed ID: 12112211 [Abstract] [Full Text] [Related]
13. Extension of the mutation spectrum in Friedreich's ataxia: detection of an exon deletion and novel missense mutations. Zühlke CH, Dalski A, Habeck M, Straube K, Hedrich K, Hoeltzenbein M, Konstanzer A, Hellenbroich Y, Schwinger E. Eur J Hum Genet; 2004 Nov 15; 12(11):979-82. PubMed ID: 15340363 [Abstract] [Full Text] [Related]
14. Trinucleotide GAA repeat expansions in seven French Friedreich ataxia families. Lucotte G, Berriche S, David F, Bathelier C, Turpin JC. Genet Couns; 1997 Nov 15; 8(3):189-94. PubMed ID: 9327260 [Abstract] [Full Text] [Related]
15. Targeting the gene in Friedreich ataxia. Hebert MD. Biochimie; 2008 Aug 15; 90(8):1131-9. PubMed ID: 18206656 [Abstract] [Full Text] [Related]
16. Founder haplotype for Machado-Joseph disease in the Indian population: novel insights from history and polymorphism studies. Mittal U, Srivastava AK, Jain S, Jain S, Mukerji M. Arch Neurol; 2005 Apr 15; 62(4):637-40. PubMed ID: 15824265 [Abstract] [Full Text] [Related]