| 000 | 01896 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250514005258.0 | ||
| 264 | 0 | _c20011004 | |
| 008 | 200110s 0 0 eng d | ||
| 022 | _a0027-8424 | ||
| 024 | 7 |
_a10.1073/pnas.181336698 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMatesic, L E | |
| 245 | 0 | 0 |
_aMutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice. _h[electronic resource] |
| 260 |
_bProceedings of the National Academy of Sciences of the United States of America _cAug 2001 |
||
| 300 |
_a10238-43 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. | ||
| 650 | 0 | 4 | _aAdaptor Proteins, Signal Transducing |
| 650 | 0 | 4 | _aAmino Acid Sequence |
| 650 | 0 | 4 | _aAnimals |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 |
_aCarrier Proteins _xgenetics |
| 650 | 0 | 4 | _aChromosome Mapping |
| 650 | 0 | 4 |
_aChromosomes, Artificial, Bacterial _xgenetics |
| 650 | 0 | 4 |
_aDNA Primers _xgenetics |
| 650 | 0 | 4 | _aGenetic Complementation Test |
| 650 | 0 | 4 |
_aMelanosomes _xmetabolism |
| 650 | 0 | 4 | _aMice |
| 650 | 0 | 4 | _aMice, Inbred C57BL |
| 650 | 0 | 4 | _aMice, Mutant Strains |
| 650 | 0 | 4 | _aMolecular Sequence Data |
| 650 | 0 | 4 | _aMultigene Family |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aPigmentation Disorders _xgenetics |
| 650 | 0 | 4 | _aSequence Homology, Amino Acid |
| 650 | 0 | 4 |
_arab GTP-Binding Proteins _xgenetics |
| 650 | 0 | 4 | _arab27 GTP-Binding Proteins |
| 700 | 1 | _aYip, R | |
| 700 | 1 | _aReuss, A E | |
| 700 | 1 | _aSwing, D A | |
| 700 | 1 | _aO'Sullivan, T N | |
| 700 | 1 | _aFletcher, C F | |
| 700 | 1 | _aCopeland, N G | |
| 700 | 1 | _aJenkins, N A | |
| 773 | 0 |
_tProceedings of the National Academy of Sciences of the United States of America _gvol. 98 _gno. 18 _gp. 10238-43 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1073/pnas.181336698 _zAvailable from publisher's website |
| 999 |
_c11430031 _d11430031 |
||