(Q42752301)
Statements
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Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome (English)
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Marta Romani
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Ichraf Kraoua
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Maria Teresa Dotti
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Mara Cavallin
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László Sztriha
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Rosario Ruta
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Francesca Mancini
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Benrhouma Hanene
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Maria Alessandra Carluccio
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Adrienn Máté
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Alíz Zimmermann
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Neziha Gouider-Khouja
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5 May 2014
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Identifiers
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