Mandibuloacral Dysplasia Is Caused by a Mutation in LMNA-Encoding Lamin A/C-Reference-Cited by-同舟云学术

Mandibuloacral Dysplasia Is Caused by a Mutation in LMNA-Encoding Lamin A/C

Published:2002-08 Issue:2 Volume:71 Page:426-431
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Novelli Giuseppe,Muchir Antoine,Sangiuolo Federica,Helbling-Leclerc Anne,D’Apice Maria Rosaria,Massart Catherine,Capon Francesca,Sbraccia Paolo,Federici Massimo,Lauro Renato,Tudisco Cosimo,Pallotta Rosanna,Scarano Gioacchino,Dallapiccola Bruno,Merlini Luciano,Bonne Gisèle

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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3. Mutations in the gene encoding lamin A/C causes autosomal dominant Emery Dreifuss muscular dystrophy;Bonne;Nat Genet,1999

4. Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy;Cao;Hum Mol Genet,2000

5. A case of cleidocranial dysostosis;Cavallazzi;Riv Clin Pediatr,1960

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