A novel small deletion in PMP22 causes a mild hereditary neuropathy with liability to pressure palsies phenotype.

Casasnovas, Carlos; Banchs, Isabel; De Jorge, Laura; Antónia Albertí, Maria; Martínez-Campo, Yolanda; Povedano, Mónica; Montero, Jordi; Volpini, Victor

Casasnovas, Carlos; Banchs, Isabel; De Jorge, Laura; Antónia Albertí, Maria; Martínez-Campo, Yolanda; Povedano, Mónica; Montero, Jordi; Volpini, Victor.

Affiliation

Casasnovas C; Neuromuscular Unit, Neurology Department, Hospital Universitari de Bellvitge, c/ Feixa Llarga s/n, 08907 L'Hospitalet de Llobregat, Barcelona, Spain. carloscasasnovas@bellvitgehospital.cat

Muscle Nerve ; 45(1): 135-8, 2012 Jan.

Article in En | MEDLINE | ID: mdl-22190321

Subject(s)

Myelin Proteins/genetics; Paralysis/genetics; Polyneuropathies/genetics; Sequence Deletion/genetics; Adult; Chromosomes, Human, Pair 17; Humans; Male; Middle Aged; Neural Conduction/genetics; Paralysis/complications; Polyneuropathies/complications

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Paralysis / Polyneuropathies / Sequence Deletion / Myelin Proteins Type of study: Etiology_studies Limits: Adult / Humans / Male / Middle aged Language: En Journal: Muscle Nerve Year: 2012 Type: Article Affiliation country: Spain

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