Skip to search formSkip to main contentSkip to account menu

DMD wt Allele

Known as: CMD3B, DXS270, DXS272 
Human DMD wild-type allele is located in the vicinity of Xp21.2 and is approximately 2225 kb in length. This allele, which encodes dystrophin protein… 
National Institutes of Health

Related topics

Related topics

11 relations
Becker Muscular DystrophyBone DensityCell MovementCytokinesis

Broader (1)

DMD gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
1996
1996
X-linked mental retardation with neonatal hypotonia in a French family (MRX15): gene assignment to Xp11.22-Xp21.1.
Linkage analysis was performed in a family with non-specific X-linked mental retardation (MRX 15). Hypotonia in infancy was the… 
1993
1993
Localization of a gene responsible for nonspecific mental retardation (MRX9) to the pericentromeric region of the X chromosome.
Nonspecific X-linked mental retardation (MRX) includes several distinct entities with mental retardation but without additional… 
1989
1989
Molecular Xp deletion in a male: suggestion of a locus for hypogonadotropic hypogonadism distal to the glycerol kinase and adrenal hypoplasia loci
We have analyzed one patient with a syndrome of glycerol kinase deficiency (GKD), adrenal hypoplasia (AH), mental retardation (MR… 
1988
1988
Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome.
We have studied patients with Duchenne muscular dystrophy (DMD), DMD together with glycerol kinase (GK) deficiency, or DMD… 
1988
1988
Localization of the X-linked retinitis pigmentosa locus between DXS7 and DXS84 in a family showing tapetal reflex in heterozygotes.
The linkage relationships between the X-linked retinitis pigmentosa (XLRP) locus and seven Xp loci: DXS14, DXS7, OTC, DXS141… 
1987
1987
Linked polymorphic DNA markers in the prediction of X‐linked muscular dystrophy
Ten polymorphic DNA markers, including gene specific markers of loci DXS164 and DXS206, were tested for allele frequencies… 
1987
1987
New RFLPs at the DXS164 (pERT 87-8) locus in the black population.
1987
1987
A small deletion in the Duchenne/Becker muscular dystrophy locus —a functionally important region?
SummaryA DNA deletion in a patient with Becker muscular dystrophy (BMD) has been delineated by restriction endonuclease mapping… 
1987
1987
Prenatal diagnosis of X-linked chronic granulomatous disease using restriction fragment length polymorphism analysis.
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)