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Mutation in FA2H leads to Fatty Acid Hydroxylase-associated Neurodegeneration (FAHN)

Kruer, MC; Paisan-Ruiz, C; Yoon, MY; Hama, H; Gregory, A; Malandrini, A; Woltjer, RL; ... Hayflick, SJ; + view all (2010) Mutation in FA2H leads to Fatty Acid Hydroxylase-associated Neurodegeneration (FAHN). In: (Proceedings) 39th Annual Meeting of the Child-Neurology-Society. (pp. S91-S91). WILEY-LISS

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Type: Proceedings paper
Title: Mutation in FA2H leads to Fatty Acid Hydroxylase-associated Neurodegeneration (FAHN)
Event: 39th Annual Meeting of the Child-Neurology-Society
Location: Providence, RI
Dates: 13 October 2010 - 16 October 2010
Keywords: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences, Neurosciences & Neurology
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Department of Neuromuscular Diseases
URI: http://discovery.ucl.ac.uk/id/eprint/1399032
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