| 000 | 01121 a2200361 4500 | ||
|---|---|---|---|
| 005 | 20250512121044.0 | ||
| 264 | 0 | _c19730904 | |
| 008 | 197309s 0 0 eng d | ||
| 022 | _a0077-0876 | ||
| 024 | 7 |
_a10.1159/000392713 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aThomas, P K | |
| 245 | 0 | 0 |
_aAutosomal dominant forms of hereditary hypertrophic neuropathy. _h[electronic resource] |
| 260 |
_bMonographs in human genetics _c1972 |
||
| 300 |
_a210 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aAge Factors |
| 650 | 0 | 4 |
_aCeramides _xmetabolism |
| 650 | 0 | 4 | _aChromosome Aberrations |
| 650 | 0 | 4 | _aChromosome Disorders |
| 650 | 0 | 4 | _aGenes, Dominant |
| 650 | 0 | 4 |
_aHexoses _xmetabolism |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aHypertrophy |
| 650 | 0 | 4 | _aMetabolism, Inborn Errors |
| 650 | 0 | 4 | _aMuscular Atrophy |
| 650 | 0 | 4 |
_aNeuritis _xgenetics |
| 650 | 0 | 4 | _aSyndrome |
| 700 | 1 | _aCalne, D B | |
| 700 | 1 | _aKing, R H | |
| 773 | 0 |
_tMonographs in human genetics _gvol. 6 _gp. 210 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1159/000392713 _zAvailable from publisher's website |
| 999 |
_c4667710 _d4667710 |
||