Bibliographic Details
| Title: |
Severe cognitive impairment in DMD: obvious clinical indication for Dp71 isoform point mutation screening. |
| Authors: |
Moizard MP; Unité de Génétique, Hôpital Bretonneau, Tours, France. moizard-m@lemel.fr, Toutain A, Fournier D, Berret F, Raynaud M, Billard C, Andres C, Moraine C |
| Source: |
European journal of human genetics : EJHG [Eur J Hum Genet] 2000 Jul; Vol. 8 (7), pp. 552-6. |
| Publication Type: |
Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: |
Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print Cited Medium: Print ISSN: 1018-4813 (Print) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE |
| Database: |
MEDLINE Ultimate |
