Human growth hormone stabilizes walking and improves strength in a patient with dominantly inherited calpainopathy
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference25 articles.
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2. Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A;Richard;Cell,1995
3. The frequency of limb girdle muscular dystrophy 2A in northeastern Italy;Fanin;Neuromuscul Disord,2005
4. A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy;Vissing;Brain,2016
5. A phase I/II trial of MYO-029 in adult subjects with muscular dystrophy;Wagner;Ann Neurol,2008
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