Further evidence supporting linkage of hereditary neuralgic amyotrophy to chromosome 17q.

Wehnert, M; Timmerman, V; Spoelders, P; Meuleman, J; Nelis, E; Van Broeckhoven, C

Wehnert, M; Timmerman, V; Spoelders, P; Meuleman, J; Nelis, E; Van Broeckhoven, C.

Afiliação

Wehnert M; Institute for Human Genetics, Ernst-Moritz-Arndt University Greifswald, Germany.

Neurology ; 48(6): 1719-21, 1997 Jun.

Article em En | MEDLINE | ID: mdl-9191796

ABSTRACT

ABSTRACT

Hereditary neuralgic amyotrophy is a rare autosomal dominant disorder of the peripheral nervous system. Previous segregation analysis in two large pedigrees suggested linkage to distal 17q. Linkage data obtained in the present study investigating a three generation pedigree confirm linkage to 17q24-q25.

Assuntos

Neurite do Plexo Braquial/genética; Cromossomos Humanos Par 17; Adolescente; Adulto; Criança; Pré-Escolar; Saúde da Família; Feminino; Ligação Genética; Marcadores Genéticos; Humanos; Lactente; Masculino; Linhagem

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Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 17 / Neurite do Plexo Braquial Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 1997 Tipo de documento: Article

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