Using Whole Genome Sequencing in an African Subphenotype of Myasthenia Gravis to Generate a Pathogenetic Hypothesis.

Nel, Melissa; Mulder, Nicola; Europa, Tarin A; Heckmann, Jeannine M

Nel, Melissa; Mulder, Nicola; Europa, Tarin A; Heckmann, Jeannine M.

Afiliação

Nel M; Neurology Research Group, Division of Neurology, Department of Medicine, University of Cape Town, Cape Town, South Africa.
Mulder N; Computational Biology Division, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South Africa.
Europa TA; Neurology Research Group, Division of Neurology, Department of Medicine, University of Cape Town, Cape Town, South Africa.
Heckmann JM; Neurology Research Group, Division of Neurology, Department of Medicine, University of Cape Town, Cape Town, South Africa.

Front Genet ; 10: 136, 2019.

Article em En | MEDLINE | ID: mdl-30881381

Palavras-chave

African; HLA-DPB1; association; extraocular muscle; extreme phenotype; myasthenia gravis; ophthalmoplegia; whole genome sequencing

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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo

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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Ano de publicação: 2019 Tipo de documento: Article