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NEW GENES AND DISEASES: EP.305 Homozygous WASHC4 variant in two sisters causes a syndromic phenotype with skeletal muscle involvement.
- Source :
-
Neuromuscular Disorders . 2021 Supplement 1, Vol. 31, pS143-S143. 1p. - Publication Year :
- 2021
- Subjects :
- *PHENOTYPES
*SKELETAL muscle
*SISTERS
*GENES
Subjects
Details
- Language :
- English
- ISSN :
- 09608966
- Volume :
- 31
- Database :
- Academic Search Index
- Journal :
- Neuromuscular Disorders
- Publication Type :
- Academic Journal
- Accession number :
- 152517362
- Full Text :
- https://doi.org/10.1016/j.nmd.2021.07.330