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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
2016
2016
Congenital Muscular Dystrophies (CMD) is the group of the neuromuscular diseases which are characterized by heavy hypotonia… Expand
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
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
Highly Cited
1996
Highly Cited
1996
We have used fluorescence in situ hybridization to establish precise chromosomal localizations for three human genes encoding… Expand