Genetics of amyotrophic lateral sclerosis: more than twenty years of studies
Amyotrophic lateral sclerosis, also known as motor neuron disease or Lou Gehrig’s disease, is an adult-onset neurodegenerative disease that targets motor neurons in the spinal cord, cortex and brain stem. Selective degeneration of corticospinal (upper) and spinal (lower) motor neurons manifests as a...
Ausführliche Beschreibung
Autor*in: |
Mazzini Letizia [verfasserIn] Marchi Fabiola De [verfasserIn] Corrado Lucia [verfasserIn] D’Alfonso Sandra [verfasserIn] |
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Englisch |
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2017 |
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In: The EuroBiotech Journal - Sciendo, 2018, 1(2017), s2, Seite 131-132 |
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volume:1 ; year:2017 ; number:s2 ; pages:131-132 |
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DOI / URN: |
10.24190/ISSN2564-615X/2017/S2.05 |
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Katalog-ID: |
DOAJ057129398 |
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10.24190/ISSN2564-615X/2017/S2.05 doi (DE-627)DOAJ057129398 (DE-599)DOAJcd2d4a26a16a457c8f6bc7e90051f9bb DE-627 ger DE-627 rakwb eng TP248.13-248.65 Mazzini Letizia verfasserin aut Genetics of amyotrophic lateral sclerosis: more than twenty years of studies 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Amyotrophic lateral sclerosis, also known as motor neuron disease or Lou Gehrig’s disease, is an adult-onset neurodegenerative disease that targets motor neurons in the spinal cord, cortex and brain stem. Selective degeneration of corticospinal (upper) and spinal (lower) motor neurons manifests as a linear decline in muscular function, eventually resulting in paralysis, speech and swallowing deficits and death, usually from impaired respiratory function, over a time course of approximately 3-5 years. als genetics lou gehrig’s disease Biotechnology Marchi Fabiola De verfasserin aut Corrado Lucia verfasserin aut D’Alfonso Sandra verfasserin aut In The EuroBiotech Journal Sciendo, 2018 1(2017), s2, Seite 131-132 (DE-627)1028957599 2564615X nnns volume:1 year:2017 number:s2 pages:131-132 https://doi.org/10.24190/ISSN2564-615X/2017/S2.05 kostenfrei https://doaj.org/article/cd2d4a26a16a457c8f6bc7e90051f9bb kostenfrei https://doi.org/10.24190/ISSN2564-615X/2017/S2.05 kostenfrei https://doaj.org/toc/2564-615X Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 1 2017 s2 131-132 |
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Amyotrophic lateral sclerosis, also known as motor neuron disease or Lou Gehrig’s disease, is an adult-onset neurodegenerative disease that targets motor neurons in the spinal cord, cortex and brain stem. Selective degeneration of corticospinal (upper) and spinal (lower) motor neurons manifests as a linear decline in muscular function, eventually resulting in paralysis, speech and swallowing deficits and death, usually from impaired respiratory function, over a time course of approximately 3-5 years. |
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Amyotrophic lateral sclerosis, also known as motor neuron disease or Lou Gehrig’s disease, is an adult-onset neurodegenerative disease that targets motor neurons in the spinal cord, cortex and brain stem. Selective degeneration of corticospinal (upper) and spinal (lower) motor neurons manifests as a linear decline in muscular function, eventually resulting in paralysis, speech and swallowing deficits and death, usually from impaired respiratory function, over a time course of approximately 3-5 years. |
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Amyotrophic lateral sclerosis, also known as motor neuron disease or Lou Gehrig’s disease, is an adult-onset neurodegenerative disease that targets motor neurons in the spinal cord, cortex and brain stem. Selective degeneration of corticospinal (upper) and spinal (lower) motor neurons manifests as a linear decline in muscular function, eventually resulting in paralysis, speech and swallowing deficits and death, usually from impaired respiratory function, over a time course of approximately 3-5 years. |
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