000 | 01228 a2200361 4500 | ||
---|---|---|---|
005 | 20250513091029.0 | ||
264 | 0 | _c19960718 | |
008 | 199607s 0 0 eng d | ||
022 | _a0006-4971 | ||
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aJenkins, M M | |
245 | 0 | 0 |
_aA novel mutation found in the 3' domain of NADH-cytochrome B5 reductase in an African-American family with type I congenital methemoglobinemia. _h[electronic resource] |
260 |
_bBlood _cApr 1996 |
||
300 |
_a2993-9 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S. | ||
650 | 0 | 4 | _aAdolescent |
650 | 0 | 4 | _aBase Sequence |
650 | 0 | 4 |
_aBlack People _xgenetics |
650 | 0 | 4 | _aCloning, Molecular |
650 | 0 | 4 |
_aCytochrome Reductases _xgenetics |
650 | 0 | 4 | _aCytochrome-B(5) Reductase |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMale |
650 | 0 | 4 |
_aMethemoglobinemia _xcongenital |
650 | 0 | 4 | _aMolecular Sequence Data |
650 | 0 | 4 | _aPedigree |
650 | 0 | 4 | _aPoint Mutation |
650 | 0 | 4 | _aSequence Analysis |
650 | 0 | 4 | _aBlack or African American |
700 | 1 | _aPrchal, J T | |
773 | 0 |
_tBlood _gvol. 87 _gno. 7 _gp. 2993-9 |
|
999 |
_c8638960 _d8638960 |