Correction: A rare homozygous missense mutation of COL7A1 in a Vietnamese family
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2054-345X
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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Correction: A rare homozygous missense mutation of COL7A1 in a Vietnamese family ; volume:9 ; number:1 ; day:6 ; month:6 ; year:2022 ; pages:1 ; date:12.2022
Human genome variation ; 9, Heft 1 (6.6.2022), 1, 12.2022
- Urheber
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Duong, Nguyen Thuy
Anh, Luong Thi Lan
Sau, Nguyen Huu
Anh, Nguyen Bao
Miyake, Noriko
Hai, Nong Van
Matsumoto, Naomichi
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1038/s41439-022-00201-0
- URN
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urn:nbn:de:101:1-2022080323172030404065
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:27 MESZ
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Beteiligte
- Duong, Nguyen Thuy
- Anh, Luong Thi Lan
- Sau, Nguyen Huu
- Anh, Nguyen Bao
- Miyake, Noriko
- Hai, Nong Van
- Matsumoto, Naomichi
- SpringerLink (Online service)
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A homozygous PIGN missense mutation in Soft-Coated Wheaten Terriers with a canine paroxysmal dyskinesia
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A rare homozygous missense mutation of COL7A1 in a Vietnamese family
Intellectual disability associated with a homozygous missense mutation in THOC6
A homozygous PIGN missense mutation in Soft-Coated Wheaten Terriers with a canine paroxysmal dyskinesia
A novel homozygous missense SLC25A20 mutation in three CACT-deficient patients: clinical and autopsy data
Sacs R272C missense homozygous mice develop an ataxia phenotype
Homozygous Missense Mutation on Exon 22 of PKHD1 Gene Causing Fatal Autosomal Recessive Polycystic Kidney Disease
Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family
Identification of a Novel Missense KRT12 Mutation in a Vietnamese Family with Meesmann Corneal Dystrophy
Missense mutation of MAL causes a rare leukodystrophy similar to Pelizaeus-Merzbacher disease
A recurrent homozygous missense DPM3 variant leads to muscle and brain disease
Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson’s disease