000 01376 a2200409 4500
005 20250517104939.0
264 0 _c20171116
008 201711s 0 0 eng d
022 _a1573-3599
024 7 _a10.1007/s10897-016-9980-7
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWei, Xianda
245 0 0 _aNotable Carrier Risks for Individuals Having Two Copies of SMN1 in Spinal Muscular Atrophy Families with 2-copy Alleles: Estimation Based on Chinese Meta-analysis Data.
_h[electronic resource]
260 _bJournal of genetic counseling
_c02 2017
300 _a72-78 p.
_bdigital
500 _aPublication Type: Journal Article; Meta-Analysis
650 0 4 _aAlleles
650 0 4 _aFemale
650 0 4 _aGene Dosage
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMuscular Atrophy, Spinal
_xgenetics
650 0 4 _aMutation
650 0 4 _aSurvival of Motor Neuron 1 Protein
_xgenetics
700 1 _aTan, Hu
700 1 _aYang, Pu
700 1 _aZhang, Rui
700 1 _aTan, Bo
700 1 _aZhang, Yue
700 1 _aMei, Libin
700 1 _aLiang, Desheng
700 1 _aWu, Lingqian
773 0 _tJournal of genetic counseling
_gvol. 26
_gno. 1
_gp. 72-78
856 4 0 _uhttps://doi.org/10.1007/s10897-016-9980-7
_zAvailable from publisher's website
999 _c26233079
_d26233079