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Crosby Andrew H.
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http://hub.abes.fr/bmj/periodical/jnnp/2001/volume_71/issue_6/B35A58F054450DA1E053120B220AC3BE/authorship/4
http://hub.abes.fr/bmj/periodical/jmg/2013/volume_50/issue_2/B35958AFB1366AAFE053120B220A26C8/authorship/15
http://hub.abes.fr/oup/periodical/brainj/2004/volume_127/issue_5/101093brainawh125/authorship/2
http://hub.abes.fr/bmj/periodical/archdischild/2007/volume_92/issue_2/B3532A3DD9924A1CE053120B220A28C4/authorship/3
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_11/B3598D6B5BE17CBEE053120B220A90C5/authorship/2
http://hub.abes.fr/oup/periodical/brainj/2010/volume_133/issue_6/101093brainawq109/authorship/10
http://hub.abes.fr/oup/periodical/brainj/2009/volume_132/issue_6/101093brainawp073/authorship/24
http://hub.abes.fr/bmj/periodical/hrt/2008/volume_94/issue_10/B357C1AA3A55065EE053120B220AEC59/authorship/9
http://hub.abes.fr/bmj/periodical/jmedgenet/2005/volume_42/issue_1/B3598D6B61F07CBEE053120B220A90C5/authorship/10
http://hub.abes.fr/springer/periodical/335/1996/volume_7/issue_2/B8CA678C38C866D6E053120B220A2E8F/authorship/1
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CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5
Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies
A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia
Mapping of the human and mouse bone sialoprotein and osteopontin loci
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