Your browser doesn't support javascript.
loading
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.
Affiliation
  • 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 in En | MEDLINE | ID: mdl-28446956
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Database: MEDLINE Language: En Journal: Hum Genome Var Year: 2017 Type: Article Affiliation country: Morocco
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Database: MEDLINE Language: En Journal: Hum Genome Var Year: 2017 Type: Article Affiliation country: Morocco