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max answer date	2015-02-10
question first answered	2014-12-02T12:42:21.587Z
house id	2
date tabled	2014-11-18

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registered interest

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answering body

answering dept id

answering dept short name

answering dept sort name

hansard heading

house id

legislature


pref label

question text

tabling member printed

uin

answer

is ministerial correction

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answer text

answering member printed

question first answered

answering member


label

tabling member


label

156464

registered interest

date

18/11/2014

answering body

Department of Health

answering dept id

answering dept short name

Health

answering dept sort name

Health

hansard heading

IVF

house id

legislature

25277

pref label	House of Lords

question text

To ask Her Majesty’s Government, further to the Written Answer by Earl Howe on 17 November (HL2642), whether they consider that any of the mitochondrial diseases listed in Annex D of the "Mitochondrial Donation" consultation document could ever arise from a nuclear gene defect; and if so, what is their assessment of the frequency with which it occurs and how that has been reflected when discussing mitochondrial diseases that may be candidates for pronuclear transfer or spindle-chromosomal complex transfer.

tabling member printed

Lord Alton of Liverpool

uin

HL2906

answer

is ministerial correction

date of answer

02/12/2014

answer text

As stated in my Written Answer of 17 November 2014 (Official Report, col. WA59) the mitochondrial diseases listed in Annex D of the mitochondrial donation consultation document are diseases caused by an inherited mutation in mitochondrial DNA. As such, none of these diseases are caused by a nuclear gene defect. Mitochondrial disorders caused by a nuclear gene defect are distinct from those listed in Annex D.

answering member printed

Earl Howe

question first answered

02/12/2014 12:42:21

answering member

2000

label	Biography information for Earl Howe

tabling member

738

label	Biography information for Lord Alton of Liverpool