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A family with autosomal dominant mutilating neuropathy not linked to either Charcot–Marie–Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci

✍ Scribed by Emilia Bellone; Carmelo Rodolico; Antonio Toscano; Emilio Di Maria; Denise Cassandrini; Antonio Pizzuti; Simona Pigullo; Anna Mazzeo; Vincenzo Macaione; Paolo Girlanda; Giuseppe Vita; Franco Ajmar; Paola Mandich


Book ID
117669492
Publisher
Elsevier Science
Year
2002
Tongue
English
Weight
144 KB
Volume
12
Category
Article
ISSN
0960-8966

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