Correction to: Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report
Abstract Following publication of the original article [1], the authors requested a correction to the details of one of the co-authors.
Saved in:
Main Authors: | Zsolt Bánfai (Author), Kinga Hadzsiev (Author), Endre Pál (Author), Katalin Komlósi (Author), Márton Melegh (Author), László Balikó (Author), Béla Melegh (Author) |
---|---|
Format: | Book |
Published: |
BMC,
2017-12-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report
by: Zsolt Bánfai, et al.
Published: (2017) -
Down-Syndrome-Related Maternal Dysbiosis Might Be Triggered by Certain Classes of Antibiotics: A New Insight into the Possible Pathomechanisms
by: Gábor Ternák, et al.
Published: (2023) -
MYH9 nephropathy
by: Taehoon Oh, et al.
Published: (2015) -
Molecular genetic investigation of hereditary breast and ovarian cancer patients in the Southern Transdanubian region: widening the mutation spectrum and searching for new pathogenic variants using next-generation methods
by: László Baráti, et al.
Published: (2024) -
Diverse cardiac phenotypes among different carriers of the same MYH7 splicing variant allele (c.732+1G>A) from a family
by: Peng Tu, et al.
Published: (2022)