A novel <i>PEX1</i> mutation in a Moroccan family with Zellweger spectrum disorders.

Bousfiha, Amale; Bakhchane, Amina; Charoute, Hicham; Riahi, Zied; Snoussi, Khalid; Rouba, Hassan; Bonnet, Crystel; Petit, Christine; Barakat, Abdelhamid

A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders.

Bousfiha, Amale; Bakhchane, Amina; Charoute, Hicham; Riahi, Zied; Snoussi, Khalid; Rouba, Hassan; Bonnet, Crystel; Petit, Christine; Barakat, Abdelhamid.

Afiliação

Bousfiha A; Human Molecular Genetics Laboratory, Institut Pasteur du Maroc, Casablanca, Morocco.
Bakhchane A; Human Molecular Genetics Laboratory, Institut Pasteur du Maroc, Casablanca, Morocco.
Charoute H; Human Molecular Genetics Laboratory, Institut Pasteur du Maroc, Casablanca, Morocco.
Riahi Z; INSERM UMRS1120, Institut de la Vision, Paris, France.
Snoussi K; UPMC-Sorbonnes Universités Paris VI, Paris, France.
Rouba H; Human Molecular Genetics Laboratory, Institut Pasteur du Maroc, Casablanca, Morocco.
Bonnet C; Human Molecular Genetics Laboratory, Institut Pasteur du Maroc, Casablanca, Morocco.
Petit C; INSERM UMRS1120, Institut de la Vision, Paris, France.
Barakat A; UPMC-Sorbonnes Universités Paris VI, Paris, France.

Hum Genome Var ; 4: 17009, 2017.

Article em En | MEDLINE | ID: mdl-28446956

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article