P70 A single in-frame deletion in the CAPN3 gene is linked to muscular dystrophy with a dominant pattern of inheritance

Authors :: R. Barresi
Julie Marsh
K. Bushby
R. Charlton
M. Henderson
John Vissing
V. Straub
Hanns Lochmüller
Judith N Hudson
Source :: Neuromuscular Disorders. 22:S26
Publication Year :: 2012
Publisher :: Elsevier BV, 2012.

Subjects :: Genetics
medicine.medical_specialty
Biology
medicine.disease
Inheritance (object-oriented programming)
Neurology
Ophthalmology
Pediatrics, Perinatology and Child Health
medicine
Frame (artificial intelligence)
Neurology (clinical)
Muscular dystrophy
Gene
Genetics (clinical)

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