Global Variome shared LOVD

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Phenotype #0000161960 Individual ID 00213497 Associated disease NEM Phenotype details were very weak (Fig. 6). Her limb involvement was asymmetric; delayed; walk Diagnosis/Initial nemaline myopathy Inheritance Familial Diagnosis/Definite NEM-4 Age/Examination - Age/Diagnosis - Age/Onset 4y Phenotype/Onset feeding difficulties Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2008-09-27 18:44:57 +02:00 (CEST) Date last edited 2012-03-04 15:57:58 +01:00 (CET)

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