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LMNA wt Allele

Known as: CMD1A, LMN1, Cardiomyopathy, Dilated 1A (Autosomal Dominant) 
Human LMNA wild-type allele is located within 1q21.2-q21.3 and is approximately 25 kb in length. This allele, which encodes lamin-A/C protein, plays… Expand
National Institutes of Health

Papers overview

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Review
2020
Review
2020
Biallelic pathogenic mutations of the LAMA2 gene result in congenital muscular dystrophy type 1A (CMD1A). The patient in this… Expand
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2018
2018
Giống le LMN1 do Th.S Đỗ Sỹ An, PGS.TS Le Quốc Doanh va cộng sự, chọn tạo từ nguồn giống Đai Loan nhập nội, được Bộ NN-PTNT ... 
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2016
2016
Congenital Muscular Dystrophies (CMD) is the group of the neuromuscular diseases which are characterized by heavy hypotonia… Expand
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2015
2015
We report the draft genome sequences of two Brucella abortus strains LMN1 and LMN2 isolated from cattle and pig. The LMN1 and… Expand
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2014
2014
Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA Acute Myeloid Leukemia (AML) results from a combination of… Expand
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Highly Cited
2000
Highly Cited
2000
The lipodystrophies are a group of disorders characterized by the absence or reduction of subcutaneous adipose tissue. Partial… Expand
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1999
1999
  • A. Kimura
  • Nihon Ika Daigaku zasshi
  • 1999
  • Corpus ID: 10395214
備考 原因遺伝子 原因遺伝子座 遺伝形式 心筋αアクチン 15q14 AD 不整脈を伴う 不明 CMD1A (CDCD1) 1p11 q11 不明 CMD1B (CMPD1) 9q13 q22 不明 CMD1C (CMPD3) 10q21 q22… Expand
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Highly Cited
1996
Highly Cited
1996
We have used fluorescence in situ hybridization to establish precise chromosomal localizations for three human genes encoding… Expand
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