Old Web
English
Sign In
Acemap
>
Paper
>
P 328. Novel Homozygous Variants Confirm SPTBN4-Related Congenital Myopathy and Expand the Clinical Phenotype
P 328. Novel Homozygous Variants Confirm SPTBN4-Related Congenital Myopathy and Expand the Clinical Phenotype
2018
Markus Buelow
David Süßmut
Jutta Köhler
Esther Gill
Laurie Smith
Markus Schuelke
Ellen Knierim
Keywords:
Congenital myopathy
Phenotype
Cancer research
Biology
SPTBN4
clinical phenotype
Pathology
Medicine
Correction
Source
Cite
Save
Machine Reading By IdeaReader
0
References
1
Citations
NaN
KQI
[]