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Homozygous deletion in CDH3 an...
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Homozygous deletion in CDH3 and hypotrichosis with juvenile macular dystrophy.
Manylion Llyfryddiaeth
Prif Awduron:
Halford, S
,
Holt, R
,
Németh, A
,
Downes, S
Fformat:
Journal article
Iaith:
English
Cyhoeddwyd:
2012
Daliadau
Disgrifiad
Eitemau Tebyg
Dangos Staff
Eitemau Tebyg
Characterization of CDH3-related congenital hypotrichosis with juvenile macular dystrophy
gan: Hull, S, et al.
Cyhoeddwyd: (2016)
Hypotrichosis and juvenile macular dystrophy caused by CDH3 mutation: A candidate disease for retinal gene therapy
gan: Singh, M, et al.
Cyhoeddwyd: (2016)
The first Japanese family of CDH3‐related hypotrichosis with juvenile macular dystrophy
gan: Takaaki Hayashi, et al.
Cyhoeddwyd: (2021-06-01)
CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
gan: Omer Karti, et al.
Cyhoeddwyd: (2017-09-01)
Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
gan: Yunqing Ren, et al.
Cyhoeddwyd: (2022-06-01)