This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

Review

. 1989 Jan;2(1):1019-29.

doi: 10.1016/0896-6273(89)90226-2.

Dystrophin abnormalities in Duchenne/Becker muscular dystrophy

E P Hoffman¹, L M Kunkel

Affiliations

PMID: 2696500
DOI: 10.1016/0896-6273(89)90226-2

Review

Dystrophin abnormalities in Duchenne/Becker muscular dystrophy

E P Hoffman et al. Neuron. 1989 Jan.

. 1989 Jan;2(1):1019-29.

doi: 10.1016/0896-6273(89)90226-2.

Authors

E P Hoffman¹, L M Kunkel

Affiliation

¹ Division of Genetics, Harvard Medical School, Howard Hughes Medical Institute, Boston, Massachusetts.

PMID: 2696500
DOI: 10.1016/0896-6273(89)90226-2

No abstract available

PubMed Disclaimer

Similar articles

Dystrophin-related muscular dystrophies.
Witkowski JA. Witkowski JA. J Child Neurol. 1989 Oct;4(4):251-71. doi: 10.1177/088307388900400403. J Child Neurol. 1989. PMID: 2571631 Review.
Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy.
Malhotra SB, Hart KA, Klamut HJ, Thomas NS, Bodrug SE, Burghes AH, Bobrow M, Harper PS, Thompson MW, Ray PN, et al. Malhotra SB, et al. Science. 1988 Nov 4;242(4879):755-9. doi: 10.1126/science.3055295. Science. 1988. PMID: 3055295
Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNA.
Upadhyaya M, Smith RA, Thomas NS, Norman AM, Harper PS. Upadhyaya M, et al. Clin Genet. 1990 Jun;37(6):456-62. doi: 10.1111/j.1399-0004.1990.tb03530.x. Clin Genet. 1990. PMID: 2200624
Dystrophin, the protein product of the Duchenne/Becker muscular dystrophy gene.
Monaco AP. Monaco AP. Trends Biochem Sci. 1989 Oct;14(10):412-5. doi: 10.1016/0968-0004(89)90290-9. Trends Biochem Sci. 1989. PMID: 2683261 Review.
Molecular genetics of Duchenne and Becker muscular dystrophy: emphasis on improved diagnosis.
Kunkel LM, Beggs AH, Hoffman EP. Kunkel LM, et al. Clin Chem. 1989 Jul;35(7 Suppl):B21-4. Clin Chem. 1989. PMID: 2663232 Review.

See all similar articles

Cited by

Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy.
McGreevy JW, Hakim CH, McIntosh MA, Duan D. McGreevy JW, et al. Dis Model Mech. 2015 Mar;8(3):195-213. doi: 10.1242/dmm.018424. Dis Model Mech. 2015. PMID: 25740330 Free PMC article. Review.
Detection of dystrophin in the postsynaptic density of rat brain and deficiency in a mouse model of Duchenne muscular dystrophy.
Kim TW, Wu K, Xu JL, Black IB. Kim TW, et al. Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11642-4. doi: 10.1073/pnas.89.23.11642. Proc Natl Acad Sci U S A. 1992. PMID: 1454857 Free PMC article.
Human dystrophin gene transfer: production and expression of a functional recombinant DNA-based gene.
Dickson G, Love DR, Davies KE, Wells KE, Piper TA, Walsh FS. Dickson G, et al. Hum Genet. 1991 Nov;88(1):53-8. doi: 10.1007/BF00204929. Hum Genet. 1991. PMID: 1959926
A family segregating a Friedreich ataxia phenotype that is not linked to the FRDA locus.
Smeyers P, Monrós E, Vílchez J, Lopez-Arlandis J, Prieto F, Palau F. Smeyers P, et al. Hum Genet. 1996 Jun;97(6):824-8. doi: 10.1007/BF02346197. Hum Genet. 1996. PMID: 8641704
Mechanical transduction by ion channels: A cautionary tale.
Sachs F. Sachs F. World J Neurol. 2015 Sep 28;5(3):74-87. doi: 10.5316/wjn.v5.i3.74. World J Neurol. 2015. PMID: 28078202 Free PMC article.

See all "Cited by" articles

Publication types

Actions

MeSH terms

Actions
Actions
Actions
Actions
Actions
Actions
Actions

Substances

Actions
Actions

LinkOut - more resources

Full Text Sources
- Elsevier Science
Other Literature Sources
- The Lens - Patent Citations Database
Medical
- MedlinePlus Health Information