Heterogeneity of nemaline myopathy cases with skeletal muscle α骯ctin gene mutations
PB Agrawal, CD Strickland, C Midgett… - Annals of …, 2004 - Wiley Online Library
Nemaline myopathy (NM) is the most common of several congenital myopathies that present
with skeletal muscle weakness and hypotonia. It is clinically heterogeneous and the …
with skeletal muscle weakness and hypotonia. It is clinically heterogeneous and the …
Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutations.
PB Agrawal, CD Strickland, C Midgett… - Annals of …, 2004 - europepmc.org
Nemaline myopathy (NM) is the most common of several congenital myopathies that present
with skeletal muscle weakness and hypotonia. It is clinically heterogeneous and the …
with skeletal muscle weakness and hypotonia. It is clinically heterogeneous and the …
Heterogeneity of nemaline myopathy cases with skeletal muscle α骯ctin gene mutations
PB Agrawal, CD Strickland, C Midgett, A Morales… - Annals of …, 2004 - cir.nii.ac.jp
抄録< jats: title> Abstract</jats: title>< jats: p> Nemaline myopathy (NM) is the most common
of several congenital myopathies that present with skeletal muscle weakness and hypotonia …
of several congenital myopathies that present with skeletal muscle weakness and hypotonia …
Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutations
PB Agrawal, CD Strickland, C Midgett… - Annals of …, 2004 - pubmed.ncbi.nlm.nih.gov
Nemaline myopathy (NM) is the most common of several congenital myopathies that present
with skeletal muscle weakness and hypotonia. It is clinically heterogeneous and the …
with skeletal muscle weakness and hypotonia. It is clinically heterogeneous and the …
Heterogeneity of nemaline myopathy cases with skeletal muscle α-actin gene mutations
PB Agrawal, CD Strickland… - Annals of …, 2004 - utsouthwestern.elsevierpure.com
Nemaline myopathy (NM) is the most common of several congenital myopathies that present
with skeletal muscle weakness and hypotonia. It is clinically heterogeneous and the …
with skeletal muscle weakness and hypotonia. It is clinically heterogeneous and the …
Heterogeneity of Nemaline Myopathy Cases with Skeletal Muscle α-Actin Gene Mutations
PB Agrawal, CD Strickland… - Annals of …, 2004 - research-repository.uwa.edu.au
Nemaline myopathy (NM) is the most common of several congenital myopathies that present
with skeletal muscle weakness and hypotonia. It is clinically heterogeneous and the …
with skeletal muscle weakness and hypotonia. It is clinically heterogeneous and the …
Heterogeneity of nemaline myopathy cases with skeletal muscle α-actin gene mutations
PB Agrawal, CD Strickland, C Midgett… - Annals of …, 2004 - pure.johnshopkins.edu
Nemaline myopathy (NM) is the most common of several congenital myopathies that present
with skeletal muscle weakness and hypotonia. It is clinically heterogeneous and the …
with skeletal muscle weakness and hypotonia. It is clinically heterogeneous and the …
[引用][C] Heterogeneity of nemaline myopathy cases with skeletal muscle α-actin gene mutations
PB AGRAWAL, CD STRICKLAND… - Annals of …, 2004 - pascal-francis.inist.fr
Heterogeneity of nemaline myopathy cases with skeletal muscle α-actin gene mutations
CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple …
CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple …