RIN2 Deficiency Results in Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis: MACS Syndrome-Reference-Cited by-同舟云学术

RIN2 Deficiency Results in Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis: MACS Syndrome

Published:2009-08 Issue:2 Volume:85 Page:254-263
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Basel-Vanagaite Lina,Sarig Ofer,Hershkovitz Dov,Fuchs-Telem Dana,Rapaport Debora,Gat Andrea,Isman Gila,Shirazi Idit,Shohat Mordechai,Enk Claes D.,Birk Efrat,Kohlhase Jürgen,Matysiak-Scholze Uta,Maya Idit,Knopf Carlos,Peffekoven Anette,Hennies Hans-Christian,Bergman Reuven,Horowitz Mia,Ishida-Yamamoto Akemi,Sprecher Eli

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference44 articles.

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5. Genetic heterogeneity of cutis laxa: a heterozygous tandem duplication within the fibulin-5 (FBLN5) gene;Markova;Am. J. Hum. Genet.,2003

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