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Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum.
Matejas, Verena; Hinkes, Bernward; Alkandari, Faisal; Al-Gazali, Lihadh; Annexstad, Ellen; Aytac, Mehmet B; Barrow, Margaret; Bláhová, Kveta; Bockenhauer, Detlef; Cheong, Hae Il; Maruniak-Chudek, Iwona; Cochat, Pierre; Dötsch, Jörg; Gajjar, Priya; Hennekam, Raoul C; Janssen, Françoise; Kagan, Mikhail; Kariminejad, Ariana; Kemper, Markus J; Koenig, Jens; Kogan, Jillene; Kroes, Hester Y; Kuwertz-Bröking, Eberhard; Lewanda, Amy F; Medeira, Ana; Muscheites, Jutta; Niaudet, Patrick; Pierson, Michel; Saggar, Anand; Seaver, Laurie; Suri, Mohnish; Tsygin, Alexey; Wühl, Elke; Zurowska, Aleksandra; Uebe, Steffen; Hildebrandt, Friedhelm; Antignac, Corinne; Zenker, Martin.
Affiliation
  • Matejas V; Institute of Human Genetics, University Hospital Erlangen, University of Erlangen-Nuremberg, Germany.
Hum Mutat ; 31(9): 992-1002, 2010 Sep.
Article in En | MEDLINE | ID: mdl-20556798
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Laminin / Genetic Predisposition to Disease / Mutation Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2010 Type: Article Affiliation country: Germany
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Laminin / Genetic Predisposition to Disease / Mutation Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2010 Type: Article Affiliation country: Germany