000 01467 a2200481 4500
005 20250513045515.0
264 0 _c19950316
008 199503s 0 0 eng d
022 _a0964-6906
024 7 _a10.1093/hmg/3.10.1907
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aNigro, V
245 0 0 _aNovel small mutations along the DMD/BMD gene associated with different phenotypes.
_h[electronic resource]
260 _bHuman molecular genetics
_cOct 1994
300 _a1907-8 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAmino Acid Sequence
650 0 4 _aBase Sequence
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aDNA Primers
650 0 4 _aDystrophin
_xgenetics
650 0 4 _aExons
650 0 4 _aGenetic Variation
650 0 4 _aHumans
650 0 4 _aIntrons
650 0 4 _aMolecular Sequence Data
650 0 4 _aMuscular Dystrophies
_xgenetics
650 0 4 _aPhenotype
650 0 4 _aPoint Mutation
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aPolymorphism, Genetic
700 1 _aNigro, G
700 1 _aEsposito, M G
700 1 _aComi, L I
700 1 _aMolinari, A M
700 1 _aPuca, G A
700 1 _aPolitano, L
773 0 _tHuman molecular genetics
_gvol. 3
_gno. 10
_gp. 1907-8
856 4 0 _uhttps://doi.org/10.1093/hmg/3.10.1907
_zAvailable from publisher's website
999 _c7849061
_d7849061