Disease #00362 (CSLE (lissencephaly, cobblestone (CSLE)))

Official abbreviation CSLE
Name lissencephaly, cobblestone (CSLE)
OMIM ID -
Inheritance -
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene TMEM5
Associated tissues -
Disease features -
Remarks -
Date created 2014-03-22 18:55:04 +01:00 (CET)
Date last edited 2015-12-07 07:11:25 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00016351 - PubMed: Vuillaumier-Barrot 2012 2-generation family, 1 affected fetus - ? France - - - - - CSLE - TMEM5 TMEM5 2 3 Johan den Dunnen
00016353 - PubMed: Vuillaumier-Barrot 2012 2-generation family, 4 affected fetuses - yes France - - - - - CSLE neuroglial ectopia within arachnoid space, abnormal cortical lamination, brain stem/cerebellar dysplasia TMEM5 TMEM5 2 3 Johan den Dunnen
00016355 - PubMed: Vuillaumier-Barrot 2012 2-generation family, 2 affected fetuses - no France - - - - - CSLE - TMEM5 TMEM5 2 4 Johan den Dunnen
00016356 - PubMed: Vuillaumier-Barrot 2012 2-generation family, 1 affected fetus - no France - - - - - CSLE - TMEM5 TMEM5 2 3 Johan den Dunnen
00016359 - PubMed: Vuillaumier-Barrot 2012 2-generation family, 1 affected fetus - no France - - - - - CSLE - TMEM5 TMEM5 2 3 Johan den Dunnen
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