Disorders


 

FHL1-Related Myofibrillar Myopathy


 

OMIM

GeneLocusProtein
FHL1Xq26.3Four and a half LIM domains protein 1

Laboratory Test Method Prenatal Carrier *
Children's Hospital of Philadelphia, Molecular Genetics Laboratory - Philadelphia, PA, USA  
Groupe Hospitalier Pitié Salpêtrière, Molecular and Cellular Cardiogenetics and Myogenetics Unit - Paris, France  

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

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