000 01585 a2200433 4500
005 20250514045656.0
264 0 _c20021224
008 200212s 0 0 eng d
022 _a0920-9964
024 7 _a10.1016/s0920-9964(02)00206-2
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMeyer, Jobst
245 0 0 _aMutational analysis of the connexin 36 gene (CX36) and exclusion of the coding sequence as a candidate region for catatonic schizophrenia in a large pedigree.
_h[electronic resource]
260 _bSchizophrenia research
_cNov 2002
300 _a87-91 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aChromosomes, Human, Pair 15
650 0 4 _aConnexins
_xgenetics
650 0 4 _aDNA Mutational Analysis
650 0 4 _aExons
_xgenetics
650 0 4 _aGene Frequency
650 0 4 _aGenetic Linkage
650 0 4 _aGenetic Predisposition to Disease
_xgenetics
650 0 4 _aHumans
650 0 4 _aIntrons
_xgenetics
650 0 4 _aMutation
650 0 4 _aOpen Reading Frames
_xgenetics
650 0 4 _aPedigree
650 0 4 _aPolymorphism, Genetic
650 0 4 _aRegulatory Sequences, Nucleic Acid
_xgenetics
650 0 4 _aSchizophrenia, Catatonic
_xgenetics
650 0 4 _aGap Junction delta-2 Protein
700 1 _aMai, Marion
700 1 _aOrtega, Gabriela
700 1 _aMössner, Rainald
700 1 _aLesch, Klaus-Peter
773 0 _tSchizophrenia research
_gvol. 58
_gno. 1
_gp. 87-91
856 4 0 _uhttps://doi.org/10.1016/s0920-9964(02)00206-2
_zAvailable from publisher's website
999 _c12175267
_d12175267