A newly discovered case of progressive muscular dystrophy caused by exon deletion mutation of Duchenne muscular dystrophy gene 12-28
J Biol Regul Homeost Agents
.
2019 Nov-Dec;33(6):1765-1767.
doi: 10.23812/19-124-L.
Authors
B T Li
#
1
,
J X Chen
#
2
,
H A Li
1
,
X Y Huang
1
Affiliations
1
Department of Pediatrics, Hainan Maternal and Child Health Hospital, Haikou, China.
2
Department of Medical Care Center, Hainan General Hospital, Haikou, China.
#
Contributed equally.
PMID:
31698894
DOI:
10.23812/19-124-L
No abstract available
Keywords:
MLPA gene analysis; creatine kinase; muscular dystrophy.
Publication types
Case Reports
Letter
MeSH terms
Dystrophin / genetics*
Exons*
Humans
Muscular Dystrophy, Duchenne / genetics*
Sequence Deletion*
Substances
DMD protein, human
Dystrophin