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Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations
by
de la Dure-Molla, Muriel
,
Quentric, Mickael
,
Yamaguti, Paulo Marcio
,
Acevedo, Ana-Carolina
,
Mighell, Alan J
,
Vikkula, Miikka
,
Huckert, Mathilde
,
Berdal, Ariane
,
Bloch-Zupan, Agnes
Published in
Orphanet journal of rare diseases
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FAM20A Gene Mutation: Amelogenesis or Ectopic Mineralization?
by
Lignon, Guilhem
,
Beres, Fleur
,
Quentric, Mickael
,
Rouzière, Stephan
,
Weil, Raphael
,
De La Dure-Molla, Muriel
,
Naveau, Adrien
,
Kozyraki, Renata
,
Dessombz, Arnaud
,
Berdal, Ariane
Published in
Frontiers in physiology
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Lack of FAM20A, Ectopic Gingival Mineralization and Chondro/Osteogenic Modifications in Enamel Renal Syndrome
by
Simancas Escorcia, Victor
,
Diarra, Abdoulaziz
,
Naveau, Adrien
,
Dessombz, Arnaud
,
Felizardo, Rufino
,
Cannaya, Vidjeacoumary
,
Chatziantoniou, Christos
,
Quentric, Mickaël
,
Vikkula, Miikka
,
Cases, Olivier
,
Berdal, Ariane
,
De La Dure-Molla, Muriel
,
Kozyraki, Renata
Published in
Frontiers in cell and developmental biology
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Frontiers In Cell And Developmental Biology
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Frontiers In Physiology
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Orphanet Journal Of Rare Diseases
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Subjects
Fam20A
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Life Sciences & Biomedicine
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Science & Technology
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Amelogenesis Imperfecta
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Enamel Renal Syndrome
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Amelogenesis Imperfecta - Genetics
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Amelogenesis Imperfecta - Pathology
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Amelogenesis Imperfecta And Gingival Fibromatosis Syndrome
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Calcification
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Cell And Developmental Biology
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Cell Biology
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Cell Death
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Colleges & Universities
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Defects
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Delayed Tooth Eruption
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Dental Enamel Proteins - Genetics
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Dentistry
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Developmental Biology
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Disease
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Enamel
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